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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HJI6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.508 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.508 |
CLV_PCSK_PC7_1 | 296 | 302 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 467 | 473 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.786 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.552 |
DEG_SCF_FBW7_1 | 244 | 249 | PF00400 | 0.547 |
DEG_SPOP_SBC_1 | 203 | 207 | PF00917 | 0.647 |
DOC_CKS1_1 | 108 | 113 | PF01111 | 0.522 |
DOC_CYCLIN_RxL_1 | 42 | 55 | PF00134 | 0.599 |
DOC_CYCLIN_yCln2_LP_2 | 3 | 9 | PF00134 | 0.579 |
DOC_MAPK_gen_1 | 334 | 344 | PF00069 | 0.670 |
DOC_PP1_RVXF_1 | 366 | 372 | PF00149 | 0.604 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.575 |
DOC_PP2B_LxvP_1 | 342 | 345 | PF13499 | 0.669 |
DOC_PP2B_LxvP_1 | 50 | 53 | PF13499 | 0.616 |
DOC_PP2B_LxvP_1 | 67 | 70 | PF13499 | 0.505 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.616 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 294 | 300 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 368 | 376 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 396 | 406 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 422 | 426 | PF00244 | 0.541 |
LIG_Actin_WH2_2 | 322 | 339 | PF00022 | 0.656 |
LIG_AP2alpha_1 | 371 | 375 | PF02296 | 0.606 |
LIG_BRCT_BRCA1_1 | 277 | 281 | PF00533 | 0.491 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.663 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.574 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.501 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.657 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.465 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.495 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.567 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.666 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.576 |
LIG_KLC1_Yacidic_2 | 218 | 223 | PF13176 | 0.572 |
LIG_LIR_Gen_1 | 112 | 122 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 162 | 171 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 186 | 197 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 469 | 473 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.557 |
LIG_MYND_1 | 169 | 173 | PF01753 | 0.512 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.606 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.506 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.507 |
LIG_SH2_PTP2 | 4 | 7 | PF00017 | 0.519 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.653 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.658 |
LIG_SH3_1 | 141 | 147 | PF00018 | 0.565 |
LIG_SH3_1 | 436 | 442 | PF00018 | 0.541 |
LIG_SH3_2 | 442 | 447 | PF14604 | 0.470 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.582 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.578 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.524 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.610 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.650 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.541 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.719 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.623 |
LIG_SH3_5 | 111 | 115 | PF00018 | 0.560 |
LIG_SUMO_SIM_anti_2 | 128 | 134 | PF11976 | 0.469 |
LIG_SUMO_SIM_anti_2 | 199 | 208 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 355 | 361 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 384 | 389 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 87 | 93 | PF11976 | 0.483 |
LIG_TYR_ITIM | 187 | 192 | PF00017 | 0.506 |
LIG_Vh1_VBS_1 | 444 | 462 | PF01044 | 0.553 |
LIG_WRC_WIRS_1 | 115 | 120 | PF05994 | 0.501 |
LIG_WW_3 | 291 | 295 | PF00397 | 0.524 |
MOD_CDC14_SPxK_1 | 291 | 294 | PF00782 | 0.524 |
MOD_CDK_SPxK_1 | 288 | 294 | PF00069 | 0.522 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.420 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.779 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.590 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.556 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.540 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.519 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.653 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.592 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.618 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.609 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.589 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.561 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.559 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.420 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.666 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.589 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.716 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.619 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.645 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.537 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.554 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.708 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.692 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.780 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.649 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.720 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.712 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.658 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.578 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.493 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.596 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.551 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.666 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.552 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.625 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.635 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.756 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.618 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.629 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.669 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.635 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.635 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.708 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.549 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.608 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.467 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.544 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.584 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.635 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.420 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.610 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.560 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.669 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.538 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.610 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.503 |
MOD_Plk_2-3 | 414 | 420 | PF00069 | 0.536 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.627 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.482 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.657 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.490 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.554 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.687 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.577 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.578 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.596 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.552 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.634 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.636 |
MOD_SUMO_rev_2 | 102 | 108 | PF00179 | 0.537 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.629 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.559 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 470 | 472 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 308 | 313 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 368 | 373 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X4R8 | Leishmania donovani | 63% | 99% |
A4I6Y1 | Leishmania infantum | 64% | 99% |
E9B203 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 99% |
Q4Q658 | Leishmania major | 63% | 100% |