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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4I9T3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 426 | 430 | PF00656 | 0.611 |
CLV_MEL_PAP_1 | 61 | 67 | PF00089 | 0.506 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.487 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 387 | 389 | PF00082 | 0.388 |
CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.643 |
DEG_SPOP_SBC_1 | 302 | 306 | PF00917 | 0.603 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 219 | 226 | PF00134 | 0.467 |
DOC_MAPK_gen_1 | 292 | 299 | PF00069 | 0.391 |
DOC_MAPK_HePTP_8 | 322 | 338 | PF00069 | 0.503 |
DOC_MAPK_HePTP_8 | 61 | 73 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 41 | 48 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 64 | 73 | PF00069 | 0.497 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.552 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.460 |
DOC_PP2B_PxIxI_1 | 16 | 22 | PF00149 | 0.539 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 147 | 156 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 235 | 241 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.564 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.489 |
LIG_eIF4E_1 | 402 | 408 | PF01652 | 0.486 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.742 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.615 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.600 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.568 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.519 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.457 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.746 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.583 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.521 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.581 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.511 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.408 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.634 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.608 |
LIG_SUMO_SIM_anti_2 | 277 | 283 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 333 | 338 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 17 | 22 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 277 | 283 | PF11976 | 0.491 |
LIG_SxIP_EBH_1 | 23 | 33 | PF03271 | 0.510 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.479 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.613 |
LIG_WW_3 | 27 | 31 | PF00397 | 0.551 |
MOD_CDK_SPK_2 | 442 | 447 | PF00069 | 0.602 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.742 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.611 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.568 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.677 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.462 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.604 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.610 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.526 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.735 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.463 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.404 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.639 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.457 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.641 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.670 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.467 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.578 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.632 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.452 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.730 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.580 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.627 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.435 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.675 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.688 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.751 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.503 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.630 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.496 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.616 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.495 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.516 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.462 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.672 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.552 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.463 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.486 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.583 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.566 |
MOD_Plk_2-3 | 345 | 351 | PF00069 | 0.641 |
MOD_Plk_2-3 | 374 | 380 | PF00069 | 0.477 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.676 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.527 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.540 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.550 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.790 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.610 |
MOD_SUMO_rev_2 | 205 | 215 | PF00179 | 0.512 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 459 | 461 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY58 | Leptomonas seymouri | 46% | 85% |
A0A3Q8II15 | Leishmania donovani | 99% | 100% |
A0A422MPI6 | Trypanosoma rangeli | 23% | 100% |
A4HBJ3 | Leishmania braziliensis | 64% | 100% |
C9ZMU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9B4U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q382 | Leishmania major | 90% | 100% |
V5BIT8 | Trypanosoma cruzi | 26% | 100% |