Protein Information

Cytoscape View

UniProt AC / UniProt ID Q15758 / AAAT_HUMAN
Protein Name Neutral amino acid transporter B(0)
Gene Name Name: SLC1A5
Organism Homo sapiens (Human)

PRO ID PR:Q15758
DAG View
PRO Name neutral amino acid transporter B(0) (human)
Definition A neutral amino acid transporter B(0) that is encoded in the genome of human.
Short Label hSLC1A5
Category organism-gene

Interactive Sequence View

Select/align proteoforms across species

Q15758 (SLC1A5) as Substrate

Site PTM Type PTM Enzyme Score Source PMID
M1 Acetylation UniProt 19413330, 22814378
S9 Phosphorylation PhosphoSitePlus
K10 Ubiquitination PhosphoSitePlus
S27 Phosphorylation PhosphoSitePlus
Y38 Phosphorylation PhosphoSitePlus
K178 Ubiquitination PhosphoSitePlus
S183 Phosphorylation PhosphoSitePlus
S194 Phosphorylation PhosphoSitePlus
S198 Phosphorylation PhosphoSitePlus
N212 N-Glycosylation UniProt 19349973
K247 Ubiquitination PhosphoSitePlus
K372 Ubiquitination PhosphoSitePlus
S493 Phosphorylation PhosphoSitePlus   UniProt 21406692, 23186163
T494 Phosphorylation phospho.ELM   PhosphoSitePlus   UniProt 18669648, 23186163
K502 Ubiquitination PhosphoSitePlus
S503 Phosphorylation phospho.ELM   PhosphoSitePlus   RLIMS-P   UniProt 18669648, 19690332, 30550624
K522 Sumoylation PhosphoSitePlus
K522 Ubiquitination PhosphoSitePlus
Y524 Phosphorylation PhosphoSitePlus
R525 Methylation PhosphoSitePlus
T532 Phosphorylation PhosphoSitePlus
S535 Phosphorylation phospho.ELM   PhosphoSitePlus   UniProt 23186163, 17081983, 18669648, ...19690332, 20068231
K537 Acetylation PhosphoSitePlus
K537 Ubiquitination PhosphoSitePlus
S539 Phosphorylation PhosphoSitePlus   UniProt 23186163
Site PTM Type PTM Enzyme Score Source PMID
S9 Phosphorylation HPRD 18578522
S198 Phosphorylation HPRD 20068231
S493 Phosphorylation HPRD 19651622, 18578522, 20068231
T494 Phosphorylation HPRD 18578522, 18669648, 20068231
S503 Phosphorylation HPRD 18669648
Y524 Phosphorylation HPRD 19901323, 18578522
T532 Phosphorylation HPRD 19413330, 18578522
S535 Phosphorylation HPRD 19651622, 18578522, 18669648, ...20068231, 17081983
S539 Phosphorylation HPRD 18578522

PTM sites affected in variants

Site Variant Source PMID Disease [Sample source]
R525 Q525 Biomuta DOID:363 / uterine cancer [ tcga ]
S535 F535 Biomuta DOID:1909 / melanoma [ icgc, tcga ]
K537 E537 Biomuta DOID:363 / uterine cancer [ icgc ]