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.
Uncharacterized Protein, Uncharacterized
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | yes | yes: 2 |
| Forrest at al. (procyclic) | yes | 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 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pescher et al. (upgregulation) | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HU27
| 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 | 0.675 |
| CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.545 |
| CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.350 |
| CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.459 |
| CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.495 |
| CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.374 |
| CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.544 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.708 |
| DOC_PP2B_PxIxI_1 | 5 | 11 | PF00149 | 0.606 |
| DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.613 |
| DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.595 |
| DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.718 |
| DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.501 |
| LIG_14-3-3_CanoR_1 | 183 | 191 | PF00244 | 0.760 |
| LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.487 |
| LIG_BIR_III_4 | 166 | 170 | PF00653 | 0.732 |
| LIG_FHA_1 | 24 | 30 | PF00498 | 0.561 |
| LIG_FHA_1 | 42 | 48 | PF00498 | 0.393 |
| LIG_FHA_1 | 65 | 71 | PF00498 | 0.507 |
| LIG_FHA_1 | 87 | 93 | PF00498 | 0.556 |
| LIG_FHA_2 | 193 | 199 | PF00498 | 0.652 |
| LIG_FHA_2 | 72 | 78 | PF00498 | 0.588 |
| LIG_LIR_Gen_1 | 13 | 21 | PF02991 | 0.539 |
| LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.518 |
| LIG_PTB_Apo_2 | 28 | 35 | PF02174 | 0.487 |
| LIG_PTB_Phospho_1 | 28 | 34 | PF10480 | 0.567 |
| LIG_SH2_CRK | 215 | 219 | PF00017 | 0.478 |
| LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.567 |
| LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.606 |
| LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.489 |
| LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.531 |
| LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.567 |
| MOD_CK2_1 | 171 | 177 | PF00069 | 0.657 |
| MOD_CK2_1 | 192 | 198 | PF00069 | 0.661 |
| MOD_CK2_1 | 71 | 77 | PF00069 | 0.568 |
| MOD_Cter_Amidation | 181 | 184 | PF01082 | 0.544 |
| MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.515 |
| MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.504 |
| MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.551 |
| MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.549 |
| MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.343 |
| MOD_GSK3_1 | 178 | 185 | PF00069 | 0.746 |
| MOD_GSK3_1 | 23 | 30 | PF00069 | 0.567 |
| MOD_GSK3_1 | 60 | 67 | PF00069 | 0.497 |
| MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.422 |
| MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.559 |
| MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.294 |
| MOD_NEK2_1 | 27 | 32 | PF00069 | 0.518 |
| MOD_NEK2_1 | 51 | 56 | PF00069 | 0.518 |
| MOD_NEK2_2 | 64 | 69 | PF00069 | 0.528 |
| MOD_PKA_2 | 169 | 175 | PF00069 | 0.704 |
| MOD_PKA_2 | 182 | 188 | PF00069 | 0.775 |
| MOD_PKA_2 | 41 | 47 | PF00069 | 0.547 |
| MOD_PKA_2 | 83 | 89 | PF00069 | 0.538 |
| MOD_PKB_1 | 200 | 208 | PF00069 | 0.751 |
| MOD_Plk_1 | 120 | 126 | PF00069 | 0.589 |
| MOD_Plk_1 | 23 | 29 | PF00069 | 0.493 |
| MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.661 |
| MOD_Plk_2-3 | 23 | 29 | PF00069 | 0.565 |
| MOD_Plk_4 | 121 | 127 | PF00069 | 0.572 |
| TRG_DiLeu_BaEn_1 | 13 | 18 | PF01217 | 0.582 |
| TRG_DiLeu_BaLyEn_6 | 214 | 219 | PF01217 | 0.537 |
| TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.484 |
| TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.567 |
| TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.724 |
| TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.567 |
| TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.359 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1P9W8 | Leptomonas seymouri | 63% | 100% |
| A0A1X0NI22 | Trypanosomatidae | 28% | 91% |
| A0A3S7WQS6 | Leishmania donovani | 100% | 100% |
| A0A422MXK0 | Trypanosoma rangeli | 31% | 100% |
| A4H5T4 | Leishmania braziliensis | 81% | 99% |
| D0A9K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
| E9AMV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 96% |
| Q4QHR9 | Leishmania major | 90% | 99% |
| V5BI56 | Trypanosoma cruzi | 32% | 100% |