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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q700
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.429 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.736 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.636 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.418 |
DOC_CKS1_1 | 429 | 434 | PF01111 | 0.623 |
DOC_CYCLIN_RxL_1 | 149 | 162 | PF00134 | 0.391 |
DOC_CYCLIN_RxL_1 | 239 | 249 | PF00134 | 0.453 |
DOC_MAPK_gen_1 | 149 | 159 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 414 | 422 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 9 | 16 | PF00069 | 0.453 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.510 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.510 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 247 | 251 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 281 | 288 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 441 | 451 | PF00244 | 0.700 |
LIG_APCC_ABBA_1 | 12 | 17 | PF00400 | 0.452 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.487 |
LIG_BIR_III_4 | 263 | 267 | PF00653 | 0.629 |
LIG_CaM_IQ_9 | 311 | 326 | PF13499 | 0.430 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.378 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.445 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.623 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.419 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.474 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.560 |
LIG_GBD_Chelix_1 | 219 | 227 | PF00786 | 0.497 |
LIG_LIR_Apic_2 | 41 | 45 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 80 | 90 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.524 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.493 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.593 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.611 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.641 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 155 | 160 | PF11976 | 0.472 |
LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.467 |
LIG_WRC_WIRS_1 | 39 | 44 | PF05994 | 0.550 |
MOD_CDC14_SPxK_1 | 453 | 456 | PF00782 | 0.600 |
MOD_CDK_SPK_2 | 267 | 272 | PF00069 | 0.606 |
MOD_CDK_SPK_2 | 436 | 441 | PF00069 | 0.634 |
MOD_CDK_SPxK_1 | 450 | 456 | PF00069 | 0.609 |
MOD_CDK_SPxxK_3 | 414 | 421 | PF00069 | 0.583 |
MOD_CDK_SPxxK_3 | 436 | 443 | PF00069 | 0.636 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.604 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.646 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.546 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.469 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.579 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.508 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.421 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.467 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.612 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.482 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.536 |
MOD_DYRK1A_RPxSP_1 | 414 | 418 | PF00069 | 0.521 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.425 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.534 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.454 |
MOD_GlcNHglycan | 215 | 219 | PF01048 | 0.550 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.562 |
MOD_GlcNHglycan | 263 | 267 | PF01048 | 0.707 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.690 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.423 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.564 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.557 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.510 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.640 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.651 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.619 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.553 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.481 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.525 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.649 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.576 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.534 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.582 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.457 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.616 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.505 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.370 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.426 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.443 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.527 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.468 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.521 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.691 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.423 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.497 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.711 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.448 |
MOD_PK_1 | 281 | 287 | PF00069 | 0.596 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.642 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.584 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.511 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.602 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.583 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.425 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.480 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.578 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.622 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.538 |
MOD_PKB_1 | 377 | 385 | PF00069 | 0.449 |
MOD_PKB_1 | 386 | 394 | PF00069 | 0.522 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.431 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.458 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.625 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.524 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.408 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.418 |
MOD_Plk_2-3 | 338 | 344 | PF00069 | 0.423 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.591 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.523 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.509 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.606 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.572 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.677 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.576 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.624 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.561 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.513 |
MOD_SUMO_for_1 | 303 | 306 | PF00179 | 0.464 |
MOD_SUMO_for_1 | 335 | 338 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 368 | 374 | PF00179 | 0.444 |
TRG_DiLeu_BaEn_1 | 239 | 244 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_1 | 306 | 311 | PF01217 | 0.439 |
TRG_DiLeu_BaEn_1 | 370 | 375 | PF01217 | 0.495 |
TRG_DiLeu_BaEn_1 | 82 | 87 | PF01217 | 0.487 |
TRG_DiLeu_LyEn_5 | 239 | 244 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.489 |
TRG_NES_CRM1_1 | 369 | 384 | PF08389 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 424 | 429 | PF00026 | 0.637 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUI5 | Leptomonas seymouri | 46% | 71% |
A0A3Q8IEH0 | Leishmania donovani | 88% | 100% |
A4HIM6 | Leishmania braziliensis | 69% | 71% |
A4I5X1 | Leishmania infantum | 88% | 100% |
E9B165 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |