As the MSP domain is involved in providing cell motility, this protein is likely involved in the same function.. Has a number of plant (E1ZCB1_CHLVA), fungal (G8B4Z0_CANPC) and animal orthologs.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 11 |
GO:0016020 | membrane | 2 | 11 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
Related structures:
AlphaFold database: E9AMV7
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022406 | membrane docking | 2 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051643 | endoplasmic reticulum localization | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0061817 | endoplasmic reticulum-plasma membrane tethering | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090158 | endoplasmic reticulum membrane organization | 5 | 1 |
GO:0140056 | organelle localization by membrane tethering | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.647 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.407 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.577 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.729 |
DOC_PP2B_PxIxI_1 | 5 | 11 | PF00149 | 0.616 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.735 |
DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.496 |
LIG_14-3-3_CanoR_1 | 174 | 182 | PF00244 | 0.791 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.483 |
LIG_BIR_III_4 | 156 | 160 | PF00653 | 0.722 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.568 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.426 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.554 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.603 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.663 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.525 |
LIG_LIR_Gen_1 | 13 | 21 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.608 |
LIG_PTB_Apo_2 | 28 | 35 | PF02174 | 0.483 |
LIG_PTB_Phospho_1 | 28 | 34 | PF10480 | 0.578 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.532 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.578 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.670 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.581 |
MOD_Cter_Amidation | 172 | 175 | PF01082 | 0.508 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.535 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.456 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.557 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.596 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.347 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.748 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.580 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.532 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.483 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.624 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.296 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.513 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.545 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.545 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.768 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.806 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.354 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.578 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.606 |
MOD_PKB_1 | 191 | 199 | PF00069 | 0.705 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.628 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.502 |
MOD_Plk_2-3 | 183 | 189 | PF00069 | 0.670 |
MOD_Plk_2-3 | 23 | 29 | PF00069 | 0.578 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.604 |
MOD_SUMO_rev_2 | 162 | 171 | PF00179 | 0.633 |
TRG_DiLeu_BaEn_1 | 13 | 18 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.578 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.753 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W8 | Leptomonas seymouri | 63% | 96% |
A0A1X0NI22 | Trypanosomatidae | 27% | 88% |
A0A3S7WQS6 | Leishmania donovani | 92% | 96% |
A0A422MXK0 | Trypanosoma rangeli | 31% | 100% |
A4H5T4 | Leishmania braziliensis | 78% | 100% |
A4HU27 | Leishmania infantum | 91% | 96% |
D0A9K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
Q4QHR9 | Leishmania major | 86% | 100% |
V5BI56 | Trypanosoma cruzi | 32% | 100% |