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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q0Y8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 424 | 428 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.730 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.435 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.447 |
DEG_MDM2_SWIB_1 | 211 | 219 | PF02201 | 0.388 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.635 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.621 |
DOC_CYCLIN_RxL_1 | 172 | 183 | PF00134 | 0.398 |
DOC_CYCLIN_RxL_1 | 254 | 265 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 338 | 348 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 366 | 374 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 340 | 348 | PF00069 | 0.424 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.757 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 187 | 194 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 303 | 307 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.533 |
LIG_Actin_WH2_2 | 241 | 259 | PF00022 | 0.481 |
LIG_AP_GAE_1 | 116 | 122 | PF02883 | 0.596 |
LIG_BIR_III_2 | 93 | 97 | PF00653 | 0.538 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.483 |
LIG_eIF4E_1 | 164 | 170 | PF01652 | 0.405 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.675 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.634 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.417 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.331 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.657 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.484 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.465 |
LIG_Integrin_RGD_1 | 85 | 87 | PF01839 | 0.744 |
LIG_Integrin_RGD_1 | 91 | 93 | PF01839 | 0.657 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.400 |
LIG_NRBOX | 343 | 349 | PF00104 | 0.425 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.383 |
LIG_SH2_GRB2like | 351 | 354 | PF00017 | 0.412 |
LIG_SH2_SRC | 351 | 354 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.518 |
LIG_SH2_STAT3 | 168 | 171 | PF00017 | 0.518 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.330 |
LIG_SH3_1 | 52 | 58 | PF00018 | 0.523 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.706 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.654 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.536 |
LIG_SUMO_SIM_anti_2 | 230 | 235 | PF11976 | 0.525 |
LIG_SUMO_SIM_anti_2 | 343 | 348 | PF11976 | 0.396 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.435 |
MOD_CDC14_SPxK_1 | 49 | 52 | PF00782 | 0.547 |
MOD_CDK_SPxK_1 | 46 | 52 | PF00069 | 0.553 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.556 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.557 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.504 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.691 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.731 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.539 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.473 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.512 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.619 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.594 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.525 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.505 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.537 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.476 |
MOD_GlcNHglycan | 383 | 387 | PF01048 | 0.509 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.504 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.698 |
MOD_GlcNHglycan | 427 | 431 | PF01048 | 0.662 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.766 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.598 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.744 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.706 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.434 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.524 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.764 |
MOD_LATS_1 | 185 | 191 | PF00433 | 0.438 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.623 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.495 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.658 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.506 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.520 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.444 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.522 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.721 |
MOD_NEK2_2 | 302 | 307 | PF00069 | 0.514 |
MOD_NEK2_2 | 421 | 426 | PF00069 | 0.600 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.531 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.739 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.519 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.518 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.537 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.755 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.518 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.434 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.578 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.708 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.495 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.553 |
TRG_DiLeu_BaEn_1 | 343 | 348 | PF01217 | 0.421 |
TRG_DiLeu_BaEn_4 | 195 | 201 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 251 | 256 | PF01217 | 0.584 |
TRG_ER_diArg_1 | 125 | 128 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.427 |
TRG_NLS_MonoExtN_4 | 33 | 39 | PF00514 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 175 | 180 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 197 | 201 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 332 | 337 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J8 | Leptomonas seymouri | 67% | 100% |
A0A0S4JG62 | Bodo saltans | 51% | 100% |
A0A1X0P1T1 | Trypanosomatidae | 54% | 100% |
A0A3Q8ILB9 | Leishmania donovani | 93% | 100% |
A0A422P583 | Trypanosoma rangeli | 56% | 100% |
A4HPU5 | Leishmania braziliensis | 79% | 100% |
A4IE48 | Leishmania infantum | 94% | 100% |
E9ATL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BQ98 | Trypanosoma cruzi | 58% | 100% |