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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HJU0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.475 |
CLV_PCSK_FUR_1 | 103 | 107 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 210 | 212 | PF00082 | 0.553 |
CLV_PCSK_PC7_1 | 158 | 164 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.517 |
CLV_Separin_Metazoa | 155 | 159 | PF03568 | 0.508 |
DOC_CKS1_1 | 243 | 248 | PF01111 | 0.496 |
DOC_CKS1_1 | 450 | 455 | PF01111 | 0.657 |
DOC_CYCLIN_RxL_1 | 403 | 412 | PF00134 | 0.518 |
DOC_MAPK_gen_1 | 20 | 26 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 287 | 295 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 287 | 295 | PF00069 | 0.524 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.499 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.404 |
DOC_USP7_MATH_2 | 375 | 381 | PF00917 | 0.553 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.731 |
LIG_14-3-3_CanoR_1 | 116 | 126 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 15 | 24 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 237 | 242 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 387 | 395 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 414 | 419 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 97 | 102 | PF00244 | 0.462 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.571 |
LIG_BRCT_BRCA1_1 | 239 | 243 | PF00533 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 214 | 224 | PF00928 | 0.440 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.523 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.530 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.496 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.401 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.390 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.367 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.565 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.489 |
LIG_FXI_DFP_1 | 224 | 228 | PF00024 | 0.506 |
LIG_LIR_Apic_2 | 240 | 246 | PF02991 | 0.502 |
LIG_LIR_Apic_2 | 394 | 400 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 152 | 161 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.650 |
LIG_Pex14_2 | 447 | 451 | PF04695 | 0.653 |
LIG_SH2_NCK_1 | 165 | 169 | PF00017 | 0.523 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.512 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.473 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.510 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.670 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.498 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.452 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.517 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.511 |
MOD_CDC14_SPxK_1 | 431 | 434 | PF00782 | 0.538 |
MOD_CDK_SPK_2 | 449 | 454 | PF00069 | 0.657 |
MOD_CDK_SPxK_1 | 428 | 434 | PF00069 | 0.548 |
MOD_CDK_SPxK_1 | 449 | 455 | PF00069 | 0.777 |
MOD_CDK_SPxxK_3 | 428 | 435 | PF00069 | 0.547 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.399 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.590 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.689 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.643 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.392 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.366 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.574 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.588 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.666 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.514 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.458 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.566 |
MOD_DYRK1A_RPxSP_1 | 428 | 432 | PF00069 | 0.550 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.667 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.605 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.444 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.500 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.511 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.488 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.487 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.539 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.688 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.709 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.734 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.543 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.609 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.659 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.678 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.522 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.560 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.649 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.589 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.529 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.597 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.740 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.649 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.437 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.368 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.568 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.387 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.365 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.496 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.550 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.632 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.567 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.517 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.521 |
MOD_NEK2_2 | 446 | 451 | PF00069 | 0.651 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.494 |
MOD_PK_1 | 237 | 243 | PF00069 | 0.564 |
MOD_PKA_1 | 15 | 21 | PF00069 | 0.621 |
MOD_PKA_1 | 414 | 420 | PF00069 | 0.586 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.711 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.676 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.635 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.618 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.609 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.465 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.467 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.532 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.660 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.498 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.665 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.596 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.621 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.645 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.543 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.777 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.730 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.613 |
TRG_DiLeu_BaEn_4 | 128 | 134 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 432 | 437 | PF01217 | 0.691 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 197 | 200 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.687 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X505 | Leishmania donovani | 62% | 88% |
A4I7A6 | Leishmania infantum | 60% | 100% |
E9B2A0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 82% |
Q4Q5V7 | Leishmania major | 63% | 100% |