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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HHX8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 22 | 26 | PF00656 | 0.431 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 494 | 498 | PF00656 | 0.349 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.577 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 364 | 366 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.523 |
DEG_APCC_DBOX_1 | 362 | 370 | PF00400 | 0.558 |
DEG_APCC_DBOX_1 | 409 | 417 | PF00400 | 0.498 |
DEG_SCF_FBW7_1 | 317 | 324 | PF00400 | 0.511 |
DEG_SCF_TRCP1_1 | 199 | 205 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.705 |
DEG_SPOP_SBC_1 | 256 | 260 | PF00917 | 0.775 |
DEG_SPOP_SBC_1 | 316 | 320 | PF00917 | 0.689 |
DOC_CYCLIN_RxL_1 | 158 | 166 | PF00134 | 0.641 |
DOC_MAPK_gen_1 | 511 | 519 | PF00069 | 0.369 |
DOC_MAPK_RevD_3 | 498 | 512 | PF00069 | 0.374 |
DOC_PP1_RVXF_1 | 144 | 150 | PF00149 | 0.657 |
DOC_PP1_RVXF_1 | 513 | 520 | PF00149 | 0.586 |
DOC_PP4_FxxP_1 | 215 | 218 | PF00568 | 0.681 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.435 |
DOC_USP7_UBL2_3 | 507 | 511 | PF12436 | 0.495 |
DOC_USP7_UBL2_3 | 518 | 522 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 15 | 21 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 174 | 183 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 97 | 102 | PF00244 | 0.532 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.700 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.618 |
LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.645 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 459 | 463 | PF00533 | 0.426 |
LIG_deltaCOP1_diTrp_1 | 428 | 437 | PF00928 | 0.595 |
LIG_deltaCOP1_diTrp_1 | 86 | 90 | PF00928 | 0.570 |
LIG_EH_1 | 555 | 559 | PF12763 | 0.592 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.689 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.593 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.558 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.684 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.477 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.555 |
LIG_LIR_Gen_1 | 460 | 470 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 86 | 94 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 513 | 517 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.475 |
LIG_MLH1_MIPbox_1 | 330 | 334 | PF16413 | 0.496 |
LIG_OCRL_FandH_1 | 462 | 474 | PF00620 | 0.564 |
LIG_PALB2_WD40_1 | 100 | 108 | PF16756 | 0.466 |
LIG_PCNA_yPIPBox_3 | 33 | 45 | PF02747 | 0.584 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.674 |
LIG_PTB_Apo_2 | 411 | 418 | PF02174 | 0.389 |
LIG_SH2_NCK_1 | 151 | 155 | PF00017 | 0.696 |
LIG_SH2_SRC | 128 | 131 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.407 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.657 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.674 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.686 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.618 |
LIG_TRAF2_1 | 36 | 39 | PF00917 | 0.595 |
LIG_UBA3_1 | 357 | 364 | PF00899 | 0.468 |
LIG_UBA3_1 | 412 | 419 | PF00899 | 0.432 |
LIG_WRC_WIRS_1 | 330 | 335 | PF05994 | 0.496 |
LIG_WRPW_2 | 528 | 531 | PF00400 | 0.597 |
MOD_CDK_SPK_2 | 10 | 15 | PF00069 | 0.498 |
MOD_CDK_SPK_2 | 98 | 103 | PF00069 | 0.456 |
MOD_CDK_SPxxK_3 | 259 | 266 | PF00069 | 0.513 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.736 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.700 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.604 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.744 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.612 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.595 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.716 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.577 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.540 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.651 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.651 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.538 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.672 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.761 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.597 |
MOD_GlcNHglycan | 341 | 345 | PF01048 | 0.729 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.476 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.578 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.591 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.485 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.652 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.634 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.619 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.748 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.725 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.621 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.471 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.631 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.461 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.651 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.542 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.676 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.638 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.714 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.673 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.577 |
MOD_NEK2_2 | 300 | 305 | PF00069 | 0.500 |
MOD_NEK2_2 | 329 | 334 | PF00069 | 0.747 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.496 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.609 |
MOD_Plk_2-3 | 121 | 127 | PF00069 | 0.496 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.742 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.496 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.528 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.642 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.728 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.706 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.681 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.694 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.453 |
MOD_SUMO_for_1 | 472 | 475 | PF00179 | 0.308 |
MOD_SUMO_rev_2 | 260 | 267 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 341 | 348 | PF00179 | 0.717 |
TRG_DiLeu_BaLyEn_6 | 407 | 412 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 512 | 517 | PF01217 | 0.476 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.510 |
TRG_NLS_MonoExtC_3 | 362 | 368 | PF00514 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 161 | 166 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 30 | 34 | PF00026 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 451 | 455 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.623 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8T0 | Leptomonas seymouri | 65% | 100% |
A0A0S4J4Z2 | Bodo saltans | 39% | 100% |
A0A1X0P580 | Trypanosomatidae | 49% | 100% |
A0A3R7NSX9 | Trypanosoma rangeli | 49% | 100% |
A0A3S7X6X9 | Leishmania donovani | 78% | 100% |
D0A676 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AHQ5 | Leishmania infantum | 78% | 100% |
E9B476 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q3V0 | Leishmania major | 76% | 100% |
V5BYJ7 | Trypanosoma cruzi | 45% | 100% |