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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B0Y3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.429 |
CLV_MEL_PAP_1 | 172 | 178 | PF00089 | 0.446 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.647 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.476 |
DEG_APCC_DBOX_1 | 500 | 508 | PF00400 | 0.454 |
DEG_MDM2_SWIB_1 | 257 | 264 | PF02201 | 0.427 |
DEG_SPOP_SBC_1 | 559 | 563 | PF00917 | 0.370 |
DOC_CYCLIN_RxL_1 | 419 | 427 | PF00134 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 201 | 207 | PF00134 | 0.422 |
DOC_MAPK_DCC_7 | 358 | 366 | PF00069 | 0.494 |
DOC_MAPK_RevD_3 | 328 | 343 | PF00069 | 0.475 |
DOC_MIT_MIM_1 | 497 | 507 | PF04212 | 0.486 |
DOC_PP1_RVXF_1 | 325 | 332 | PF00149 | 0.407 |
DOC_PP1_RVXF_1 | 410 | 417 | PF00149 | 0.415 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.413 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.573 |
DOC_PP4_FxxP_1 | 308 | 311 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 416 | 419 | PF00568 | 0.376 |
DOC_SPAK_OSR1_1 | 327 | 331 | PF12202 | 0.342 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.618 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.674 |
LIG_14-3-3_CanoR_1 | 290 | 294 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 423 | 432 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 532 | 538 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 54 | 62 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.627 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.396 |
LIG_BIR_III_2 | 346 | 350 | PF00653 | 0.583 |
LIG_BIR_III_4 | 227 | 231 | PF00653 | 0.409 |
LIG_CaM_NSCaTE_8 | 52 | 59 | PF13499 | 0.481 |
LIG_Clathr_ClatBox_1 | 263 | 267 | PF01394 | 0.323 |
LIG_CSL_BTD_1 | 416 | 419 | PF09270 | 0.435 |
LIG_deltaCOP1_diTrp_1 | 259 | 266 | PF00928 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 455 | 464 | PF00928 | 0.414 |
LIG_eIF4E_1 | 17 | 23 | PF01652 | 0.467 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.509 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.661 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.482 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.441 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.444 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.498 |
LIG_Integrin_isoDGR_2 | 353 | 355 | PF01839 | 0.679 |
LIG_LIR_Apic_2 | 119 | 125 | PF02991 | 0.600 |
LIG_LIR_Apic_2 | 306 | 311 | PF02991 | 0.570 |
LIG_LIR_Apic_2 | 415 | 419 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 302 | 311 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 496 | 504 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 584 | 592 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 496 | 500 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 584 | 589 | PF02991 | 0.496 |
LIG_NBox_RRM_1 | 266 | 276 | PF00076 | 0.449 |
LIG_Pex14_2 | 257 | 261 | PF04695 | 0.449 |
LIG_SH2_SRC | 586 | 589 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.448 |
LIG_SH3_2 | 126 | 131 | PF14604 | 0.380 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.428 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.728 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.486 |
LIG_SUMO_SIM_anti_2 | 26 | 35 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 560 | 570 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 156 | 163 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 336 | 341 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 362 | 368 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 579 | 584 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 61 | 67 | PF11976 | 0.459 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.492 |
LIG_TRAF2_1 | 277 | 280 | PF00917 | 0.565 |
LIG_TRAF2_1 | 600 | 603 | PF00917 | 0.511 |
LIG_WW_3 | 124 | 128 | PF00397 | 0.504 |
MOD_CDC14_SPxK_1 | 128 | 131 | PF00782 | 0.542 |
MOD_CDK_SPK_2 | 394 | 399 | PF00069 | 0.465 |
MOD_CDK_SPxK_1 | 125 | 131 | PF00069 | 0.549 |
MOD_CDK_SPxxK_3 | 415 | 422 | PF00069 | 0.456 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.741 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.508 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.473 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.460 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.375 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.526 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.448 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.593 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.460 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.415 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.515 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.510 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.379 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.451 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.622 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.658 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.297 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.614 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.652 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.541 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.481 |
MOD_GlcNHglycan | 593 | 597 | PF01048 | 0.478 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.583 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.648 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.538 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.606 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.626 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.615 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.660 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.564 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.553 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.660 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.739 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.514 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.493 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.565 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.567 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.379 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.366 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.441 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.394 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.485 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.511 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.466 |
MOD_PIKK_1 | 480 | 486 | PF00454 | 0.333 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.503 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.530 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.513 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.663 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.646 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.563 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.447 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.647 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.536 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.654 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.452 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.481 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.622 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.378 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.481 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.473 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.668 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.538 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.532 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.565 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.330 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.586 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.495 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.506 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.455 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.412 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.669 |
MOD_SUMO_for_1 | 132 | 135 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 465 | 471 | PF00179 | 0.471 |
TRG_DiLeu_BaEn_1 | 135 | 140 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 259 | 264 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_4 | 279 | 285 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 168 | 173 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 420 | 425 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.531 |
TRG_NES_CRM1_1 | 282 | 294 | PF08389 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 342 | 346 | PF00026 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P209 | Trypanosomatidae | 33% | 100% |
A0A3S5H7N2 | Leishmania donovani | 94% | 100% |
A4HIE2 | Leishmania braziliensis | 84% | 100% |
A4I5N9 | Leishmania infantum | 94% | 100% |
Q4Q783 | Leishmania major | 92% | 100% |
V5BL95 | Trypanosoma cruzi | 35% | 100% |