MCSP_HUMAN - dbPTM
MCSP_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID MCSP_HUMAN
UniProt AC P49901
Protein Name Sperm mitochondrial-associated cysteine-rich protein
Gene Name SMCP
Organism Homo sapiens (Human).
Sequence Length 116
Subcellular Localization Cytoplasm. Mitochondrion membrane
Peripheral membrane protein
Cytoplasmic side . Becomes associated with the spermatid mitochondrion capsule at step 16 of spermatogenesis..
Protein Description Involved in sperm motility. Its absence is associated with genetic background dependent male infertility. Infertility may be due to reduced sperm motility in the female reproductive tract and inability to penetrate the oocyte zona pellucida (By similarity)..
Protein Sequence MCDQTKHSKCCPAKGNQCCPPQQNQCCQSKGNQCCPPKQNQCCQPKGSQCCPPKHNHCCQPKPPCCIQARCCGLETKPEVSPLNMESEPNSPQTQDKGCQTQQQPHSPQNESRPSK
Overview of Protein Modification Sites with Functional and Structural Information
Experimental Post-Translational Modification Sites

* ASA = Accessible Surface Area

Locations Modification Substrate Peptides
&
Secondary Structure
ASA (%) Reference Orthologous
Protein Cluster
48PhosphorylationQCCQPKGSQCCPPKH
CCCCCCCCCCCCCCC
26.6029396449
91PhosphorylationNMESEPNSPQTQDKG
CCCCCCCCCCCCCCC
29.1522210691
94PhosphorylationSEPNSPQTQDKGCQT
CCCCCCCCCCCCCCC
41.9622210691

Upstream regulatory proteins (kinases for phosphorylation sites, E3 ubiquitin ligases of ubiquitination sites, ...)
Modified Location Modified Residue Modification Type of Upstream Proteins Gene Name of Upstream Proteins UniProt AC of Upstream Proteins Sources

Oops, there are no upstream regulatory protein records of MCSP_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of MCSP_HUMAN !!

Disease-associated PTM Sites based on SAP

* Distance = the distance between SAP position and PTM sites.

Modified Location Modification Variant Position
(Distance <= 10)
Residue Change SAP Related Disease Reference

Oops, there are no SNP-PTM records of MCSP_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
KR412_HUMANKRTAP4-12physical
16189514
PLS1_HUMANPLSCR1physical
16189514
ITF2_HUMANTCF4physical
25416956
CACO2_HUMANCALCOCO2physical
25416956
RGS17_HUMANRGS17physical
25416956
KR412_HUMANKRTAP4-12physical
25416956
KRA92_HUMANKRTAP9-2physical
25416956
KRA94_HUMANKRTAP9-4physical
25416956
LCE4A_HUMANLCE4Aphysical
25416956
KR107_HUMANKRTAP10-7physical
25416956
KR109_HUMANKRTAP10-9physical
25416956
KR108_HUMANKRTAP10-8physical
25416956
KR103_HUMANKRTAP10-3physical
25416956
NT2NL_HUMANNOTCH2NLphysical
25416956
KRA56_HUMANKRTAP5-6physical
25416956
KR411_HUMANKRTAP4-11physical
25416956

Drug and Disease Associations
Kegg Drug
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of MCSP_HUMAN

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Related Literatures of Post-Translational Modification

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