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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 10 |
GO:0016020 | membrane | 2 | 10 |
GO:0031090 | organelle membrane | 3 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
Related structures:
AlphaFold database: A4H5T4
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_NRD_NRD_1 | 183 | 185 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.503 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.599 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.768 |
DOC_MAPK_RevD_3 | 186 | 200 | PF00069 | 0.646 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.669 |
DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.499 |
LIG_14-3-3_CanoR_1 | 183 | 189 | PF00244 | 0.829 |
LIG_14-3-3_CanoR_1 | 201 | 210 | PF00244 | 0.771 |
LIG_14-3-3_CanoR_1 | 213 | 223 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.523 |
LIG_BIR_III_4 | 165 | 169 | PF00653 | 0.723 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.619 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.572 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.428 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.523 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.582 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.715 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.557 |
LIG_LIR_Gen_1 | 13 | 21 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.421 |
LIG_PTB_Apo_2 | 28 | 35 | PF02174 | 0.499 |
LIG_PTB_Phospho_1 | 28 | 34 | PF10480 | 0.582 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.726 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.554 |
LIG_Sin3_3 | 226 | 233 | PF02671 | 0.332 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.582 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.666 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.645 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.723 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.585 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.485 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.476 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.564 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.382 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.743 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.585 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.510 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.516 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.553 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.428 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.299 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.526 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.552 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.549 |
MOD_PKA_1 | 200 | 206 | PF00069 | 0.634 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.813 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.634 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.560 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.580 |
MOD_PKB_1 | 200 | 208 | PF00069 | 0.753 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.599 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.518 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.723 |
MOD_Plk_2-3 | 23 | 29 | PF00069 | 0.582 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.679 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.684 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.661 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.579 |
TRG_DiLeu_BaEn_1 | 13 | 18 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.765 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W8 | Leptomonas seymouri | 65% | 100% |
A0A1X0NI22 | Trypanosomatidae | 29% | 91% |
A0A3S7WQS6 | Leishmania donovani | 81% | 100% |
A0A422MXK0 | Trypanosoma rangeli | 30% | 100% |
A4HU27 | Leishmania infantum | 81% | 100% |
E9AMV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QHR9 | Leishmania major | 76% | 98% |
V5BI56 | Trypanosoma cruzi | 32% | 100% |