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: A4HKZ7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 147 | 153 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.649 |
CLV_Separin_Metazoa | 93 | 97 | PF03568 | 0.575 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.493 |
DEG_APCC_DBOX_1 | 478 | 486 | PF00400 | 0.485 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.595 |
DEG_SPOP_SBC_1 | 341 | 345 | PF00917 | 0.577 |
DEG_SPOP_SBC_1 | 362 | 366 | PF00917 | 0.621 |
DOC_CKS1_1 | 163 | 168 | PF01111 | 0.532 |
DOC_CYCLIN_RxL_1 | 422 | 432 | PF00134 | 0.616 |
DOC_CYCLIN_RxL_1 | 476 | 483 | PF00134 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 13 | 19 | PF00134 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 481 | 487 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 240 | 248 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 472 | 480 | PF00069 | 0.556 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.590 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.310 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.511 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.514 |
DOC_PP2B_LxvP_1 | 531 | 534 | PF13499 | 0.636 |
DOC_PP4_FxxP_1 | 163 | 166 | PF00568 | 0.525 |
DOC_PP4_FxxP_1 | 233 | 236 | PF00568 | 0.549 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.799 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.705 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.355 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 143 | 147 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 220 | 225 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 472 | 476 | PF00244 | 0.627 |
LIG_Actin_WH2_2 | 376 | 393 | PF00022 | 0.391 |
LIG_AP2alpha_2 | 231 | 233 | PF02296 | 0.558 |
LIG_APCC_ABBA_1 | 164 | 169 | PF00400 | 0.531 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.527 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.471 |
LIG_Clathr_ClatBox_1 | 189 | 193 | PF01394 | 0.514 |
LIG_eIF4E_1 | 287 | 293 | PF01652 | 0.318 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.586 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.660 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.384 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.541 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.489 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.591 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.524 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.506 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.636 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.515 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.568 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.559 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.652 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.432 |
LIG_LIR_Apic_2 | 160 | 166 | PF02991 | 0.524 |
LIG_LIR_Apic_2 | 231 | 236 | PF02991 | 0.420 |
LIG_LIR_Apic_2 | 247 | 253 | PF02991 | 0.438 |
LIG_LIR_Apic_2 | 284 | 290 | PF02991 | 0.526 |
LIG_LIR_Apic_2 | 300 | 304 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 22 | 33 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.504 |
LIG_MAD2 | 6 | 14 | PF02301 | 0.669 |
LIG_NRBOX | 292 | 298 | PF00104 | 0.550 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.530 |
LIG_REV1ctd_RIR_1 | 224 | 231 | PF16727 | 0.461 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.485 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.491 |
LIG_SH2_GRB2like | 334 | 337 | PF00017 | 0.433 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.433 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.567 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.425 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.660 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.768 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.578 |
LIG_SUMO_SIM_anti_2 | 244 | 250 | PF11976 | 0.557 |
LIG_SUMO_SIM_anti_2 | 36 | 41 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 188 | 197 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 85 | 90 | PF11976 | 0.395 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.612 |
LIG_TRAF2_1 | 154 | 157 | PF00917 | 0.644 |
LIG_TRAF2_1 | 558 | 561 | PF00917 | 0.440 |
LIG_UBA3_1 | 513 | 519 | PF00899 | 0.618 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.613 |
LIG_WW_1 | 14 | 17 | PF00397 | 0.399 |
MOD_CDC14_SPxK_1 | 506 | 509 | PF00782 | 0.479 |
MOD_CDK_SPK_2 | 503 | 508 | PF00069 | 0.591 |
MOD_CDK_SPK_2 | 87 | 92 | PF00069 | 0.332 |
MOD_CDK_SPxK_1 | 503 | 509 | PF00069 | 0.462 |
MOD_CDK_SPxxK_3 | 472 | 479 | PF00069 | 0.525 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.608 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.305 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.711 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.619 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.416 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.683 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.377 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.483 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.580 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.492 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.415 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.619 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.559 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.551 |
MOD_CMANNOS | 307 | 310 | PF00535 | 0.423 |
MOD_DYRK1A_RPxSP_1 | 61 | 65 | PF00069 | 0.780 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.390 |
MOD_GlcNHglycan | 177 | 181 | PF01048 | 0.641 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.731 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.630 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.751 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.643 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.513 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.784 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.554 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.472 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.632 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.787 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.348 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.675 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.528 |
MOD_LATS_1 | 340 | 346 | PF00433 | 0.505 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.564 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.614 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.457 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.570 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.538 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.573 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.548 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.489 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.580 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.710 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.525 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.614 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.651 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.361 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.349 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.691 |
MOD_Plk_2-3 | 372 | 378 | PF00069 | 0.597 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.528 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.490 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.400 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.637 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.554 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.524 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.367 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.688 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.515 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.595 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.665 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.566 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.536 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.559 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.690 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.553 |
MOD_SUMO_rev_2 | 148 | 153 | PF00179 | 0.444 |
TRG_DiLeu_BaEn_1 | 244 | 249 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_1 | 381 | 386 | PF01217 | 0.332 |
TRG_DiLeu_BaEn_2 | 254 | 260 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.311 |
TRG_DiLeu_BaLyEn_6 | 476 | 481 | PF01217 | 0.676 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.423 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2P3 | Leptomonas seymouri | 38% | 100% |
A0A0S4JT50 | Bodo saltans | 23% | 100% |
A0A3Q8IFU0 | Leishmania donovani | 72% | 100% |
A4I8H7 | Leishmania infantum | 72% | 100% |
E9B3D7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4Q4R5 | Leishmania major | 70% | 100% |