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: A0A3Q8IEH0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.599 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.525 |
CLV_PCSK_FUR_1 | 384 | 388 | PF00082 | 0.524 |
CLV_PCSK_FUR_1 | 52 | 56 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.719 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.533 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.663 |
DOC_CYCLIN_RxL_1 | 237 | 247 | PF00134 | 0.493 |
DOC_MAPK_gen_1 | 149 | 159 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 9 | 16 | PF00069 | 0.517 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.548 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 245 | 249 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 279 | 286 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 337 | 341 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 439 | 449 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 52 | 58 | PF00244 | 0.696 |
LIG_APCC_ABBA_1 | 12 | 17 | PF00400 | 0.520 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.577 |
LIG_BIR_III_4 | 261 | 265 | PF00653 | 0.707 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.580 |
LIG_CaM_IQ_9 | 309 | 324 | PF13499 | 0.474 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.489 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.686 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.515 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.653 |
LIG_GBD_Chelix_1 | 217 | 225 | PF00786 | 0.582 |
LIG_Integrin_isoDGR_2 | 185 | 187 | PF01839 | 0.708 |
LIG_LIR_Apic_2 | 41 | 45 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 80 | 90 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.518 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.500 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.707 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.653 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.769 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.732 |
LIG_SUMO_SIM_anti_2 | 155 | 160 | PF11976 | 0.557 |
LIG_SUMO_SIM_par_1 | 43 | 49 | PF11976 | 0.533 |
LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.508 |
LIG_WRC_WIRS_1 | 39 | 44 | PF05994 | 0.657 |
MOD_CDC14_SPxK_1 | 451 | 454 | PF00782 | 0.624 |
MOD_CDK_SPK_2 | 265 | 270 | PF00069 | 0.643 |
MOD_CDK_SPK_2 | 434 | 439 | PF00069 | 0.712 |
MOD_CDK_SPxK_1 | 448 | 454 | PF00069 | 0.635 |
MOD_CDK_SPxxK_3 | 412 | 419 | PF00069 | 0.650 |
MOD_CDK_SPxxK_3 | 434 | 441 | PF00069 | 0.709 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.751 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.691 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.653 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.513 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.650 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.522 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.691 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.529 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.531 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.627 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.642 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.501 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.663 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.680 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.749 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.728 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.504 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.615 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.594 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.717 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.690 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.653 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.592 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.620 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.568 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.697 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.603 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.649 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.659 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.532 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.657 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.551 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.388 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.466 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.486 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.469 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.605 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.566 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.598 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.604 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.705 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.470 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.538 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.560 |
MOD_PK_1 | 279 | 285 | PF00069 | 0.684 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.567 |
MOD_PKA_1 | 386 | 392 | PF00069 | 0.511 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.566 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.638 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.627 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.467 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.521 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.552 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.637 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.662 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.595 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.633 |
MOD_PKB_1 | 375 | 383 | PF00069 | 0.489 |
MOD_PKB_1 | 384 | 392 | PF00069 | 0.563 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.517 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.759 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.564 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.700 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.552 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.643 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.620 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.531 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.723 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.620 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.662 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.577 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.546 |
MOD_SUMO_for_1 | 301 | 304 | PF00179 | 0.548 |
MOD_SUMO_for_1 | 333 | 336 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 366 | 372 | PF00179 | 0.530 |
TRG_DiLeu_BaEn_1 | 237 | 242 | PF01217 | 0.506 |
TRG_DiLeu_BaEn_1 | 304 | 309 | PF01217 | 0.477 |
TRG_DiLeu_BaEn_1 | 368 | 373 | PF01217 | 0.612 |
TRG_DiLeu_BaEn_1 | 82 | 87 | PF01217 | 0.505 |
TRG_DiLeu_LyEn_5 | 237 | 242 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 384 | 387 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.522 |
TRG_NES_CRM1_1 | 367 | 382 | PF08389 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 370 | 374 | PF00026 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 422 | 427 | PF00026 | 0.718 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUI5 | Leptomonas seymouri | 46% | 71% |
A4HIM6 | Leishmania braziliensis | 70% | 100% |
A4I5X1 | Leishmania infantum | 100% | 100% |
E9B165 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q700 | Leishmania major | 88% | 100% |