Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S7X3N1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.479 |
CLV_PCSK_FUR_1 | 20 | 24 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.372 |
DEG_SPOP_SBC_1 | 131 | 135 | PF00917 | 0.479 |
DOC_PP1_RVXF_1 | 108 | 114 | PF00149 | 0.339 |
DOC_PP1_RVXF_1 | 33 | 39 | PF00149 | 0.374 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.585 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 178 | 185 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 199 | 205 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 84 | 94 | PF00244 | 0.391 |
LIG_14-3-3_CterR_2 | 296 | 300 | PF00244 | 0.441 |
LIG_Actin_WH2_2 | 72 | 88 | PF00022 | 0.476 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.491 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.354 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.405 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.439 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.369 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.391 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.540 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.364 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.471 |
LIG_NRBOX | 264 | 270 | PF00104 | 0.468 |
LIG_SH2_NCK_1 | 235 | 239 | PF00017 | 0.383 |
LIG_SUMO_SIM_anti_2 | 143 | 153 | PF11976 | 0.393 |
LIG_SUMO_SIM_anti_2 | 247 | 252 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 5 | 13 | PF11976 | 0.517 |
LIG_SUMO_SIM_anti_2 | 62 | 68 | PF11976 | 0.562 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.595 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.535 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.361 |
LIG_UBA3_1 | 146 | 154 | PF00899 | 0.475 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.630 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.554 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.413 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.598 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.470 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.512 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.396 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.495 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.687 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.635 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.602 |
MOD_GlcNHglycan | 219 | 224 | PF01048 | 0.554 |
MOD_GlcNHglycan | 5 | 9 | PF01048 | 0.426 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.505 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.567 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.487 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.516 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.531 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.395 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.377 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.549 |
MOD_NEK2_2 | 200 | 205 | PF00069 | 0.486 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.394 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.409 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.581 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.602 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.387 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.607 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.424 |
MOD_SUMO_for_1 | 150 | 153 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 227 | 233 | PF00179 | 0.419 |
MOD_SUMO_rev_2 | 28 | 37 | PF00179 | 0.512 |
TRG_DiLeu_BaEn_1 | 145 | 150 | PF01217 | 0.468 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 42 | 47 | PF01217 | 0.490 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDE9 | Leptomonas seymouri | 46% | 96% |
A0A1X0P1M8 | Trypanosomatidae | 28% | 100% |
A0A422NW57 | Trypanosoma rangeli | 30% | 100% |
A4HIG9 | Leishmania braziliensis | 78% | 100% |
A4I5R6 | Leishmania infantum | 100% | 100% |
C9ZR34 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B111 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q755 | Leishmania major | 92% | 100% |
V5BGW1 | Trypanosoma cruzi | 32% | 100% |