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: Q4QFT5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.467 |
CLV_C14_Caspase3-7 | 349 | 353 | PF00656 | 0.517 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 129 | 131 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.455 |
CLV_Separin_Metazoa | 38 | 42 | PF03568 | 0.610 |
DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.573 |
DEG_ODPH_VHL_1 | 150 | 163 | PF01847 | 0.434 |
DEG_SCF_FBW7_1 | 468 | 474 | PF00400 | 0.525 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.539 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.523 |
DOC_CKS1_1 | 468 | 473 | PF01111 | 0.531 |
DOC_CYCLIN_RxL_1 | 388 | 398 | PF00134 | 0.567 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.567 |
DOC_PP4_FxxP_1 | 362 | 365 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.523 |
DOC_USP7_UBL2_3 | 388 | 392 | PF12436 | 0.449 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 155 | 165 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 179 | 188 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 19 | 26 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 354 | 358 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 380 | 384 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 441 | 449 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 73 | 79 | PF00244 | 0.591 |
LIG_Actin_WH2_2 | 139 | 157 | PF00022 | 0.433 |
LIG_Actin_WH2_2 | 326 | 343 | PF00022 | 0.507 |
LIG_Actin_WH2_2 | 364 | 382 | PF00022 | 0.411 |
LIG_BIR_III_2 | 265 | 269 | PF00653 | 0.669 |
LIG_BIR_III_4 | 225 | 229 | PF00653 | 0.618 |
LIG_CaM_IQ_9 | 165 | 181 | PF13499 | 0.464 |
LIG_Dynein_DLC8_1 | 39 | 45 | PF01221 | 0.678 |
LIG_EVH1_2 | 255 | 259 | PF00568 | 0.523 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.515 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.593 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.374 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.647 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.553 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.475 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.662 |
LIG_GBD_Chelix_1 | 510 | 518 | PF00786 | 0.534 |
LIG_LIR_Apic_2 | 361 | 365 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.639 |
LIG_NRBOX | 346 | 352 | PF00104 | 0.556 |
LIG_PDZ_Class_1 | 543 | 548 | PF00595 | 0.541 |
LIG_SH2_CRK | 507 | 511 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 312 | 315 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.450 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.614 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.658 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.668 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.596 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 209 | 215 | PF11976 | 0.431 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.460 |
LIG_TRAF2_1 | 372 | 375 | PF00917 | 0.483 |
LIG_TRAF2_1 | 499 | 502 | PF00917 | 0.445 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.730 |
MOD_CDK_SPxK_1 | 445 | 451 | PF00069 | 0.603 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.567 |
MOD_CDK_SPxxK_3 | 445 | 452 | PF00069 | 0.588 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.598 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.582 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.654 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.661 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.674 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.562 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.692 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.650 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.491 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.521 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.565 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.540 |
MOD_Cter_Amidation | 71 | 74 | PF01082 | 0.592 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.545 |
MOD_GlcNHglycan | 221 | 225 | PF01048 | 0.617 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.546 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.603 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.525 |
MOD_GlcNHglycan | 436 | 440 | PF01048 | 0.537 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.636 |
MOD_GlcNHglycan | 464 | 468 | PF01048 | 0.565 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.509 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.616 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.656 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.635 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.607 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.711 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.741 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.511 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.658 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.611 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.536 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.663 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.563 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.584 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.563 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.604 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.577 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.574 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.451 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.781 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.712 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.577 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.523 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.677 |
MOD_PK_1 | 260 | 266 | PF00069 | 0.547 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.611 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.632 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.570 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.535 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.594 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.446 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.543 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.375 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.677 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.653 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.611 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.524 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.662 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.500 |
MOD_Plk_2-3 | 305 | 311 | PF00069 | 0.468 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.595 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.658 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.639 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.520 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.477 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.692 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.540 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.806 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.520 |
MOD_SUMO_for_1 | 133 | 136 | PF00179 | 0.569 |
TRG_DiLeu_BaEn_1 | 128 | 133 | PF01217 | 0.517 |
TRG_DiLeu_BaEn_1 | 296 | 301 | PF01217 | 0.527 |
TRG_DiLeu_BaEn_4 | 374 | 380 | PF01217 | 0.462 |
TRG_DiLeu_LyEn_5 | 296 | 301 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.616 |
TRG_ER_diArg_1 | 130 | 132 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 259 | 262 | PF00400 | 0.615 |
TRG_NES_CRM1_1 | 291 | 304 | PF08389 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 130 | 135 | PF00026 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 299 | 304 | PF00026 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 488 | 492 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 512 | 517 | PF00026 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 523 | 527 | PF00026 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9D0 | Leptomonas seymouri | 36% | 81% |
A0A3S7WSW7 | Leishmania donovani | 86% | 100% |
A4H6I2 | Leishmania braziliensis | 62% | 82% |
A4HVZ2 | Leishmania infantum | 86% | 100% |
E9APP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 83% |