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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9ATA4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0016192 | vesicle-mediated transport | 4 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.691 |
CLV_MEL_PAP_1 | 61 | 67 | PF00089 | 0.296 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.390 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.489 |
CLV_Separin_Metazoa | 244 | 248 | PF03568 | 0.642 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.596 |
DEG_SPOP_SBC_1 | 458 | 462 | PF00917 | 0.581 |
DOC_ANK_TNKS_1 | 435 | 442 | PF00023 | 0.606 |
DOC_CKS1_1 | 152 | 157 | PF01111 | 0.683 |
DOC_CYCLIN_RxL_1 | 369 | 376 | PF00134 | 0.570 |
DOC_CYCLIN_yCln2_LP_2 | 409 | 415 | PF00134 | 0.586 |
DOC_MAPK_FxFP_2 | 37 | 40 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 232 | 239 | PF00069 | 0.611 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.567 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.564 |
DOC_PP2B_LxvP_1 | 307 | 310 | PF13499 | 0.524 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.585 |
DOC_PP2B_LxvP_1 | 455 | 458 | PF13499 | 0.619 |
DOC_PP2B_LxvP_1 | 512 | 515 | PF13499 | 0.736 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.656 |
DOC_PP4_FxxP_1 | 279 | 282 | PF00568 | 0.560 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.421 |
DOC_PP4_FxxP_1 | 481 | 484 | PF00568 | 0.425 |
DOC_SPAK_OSR1_1 | 64 | 68 | PF12202 | 0.296 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.324 |
DOC_USP7_UBL2_3 | 406 | 410 | PF12436 | 0.658 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.324 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 227 | 235 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 365 | 374 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 471 | 476 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 76 | 85 | PF00244 | 0.364 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.550 |
LIG_deltaCOP1_diTrp_1 | 467 | 476 | PF00928 | 0.478 |
LIG_eIF4E_1 | 122 | 128 | PF01652 | 0.347 |
LIG_eIF4E_1 | 505 | 511 | PF01652 | 0.592 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.334 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.534 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.432 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.658 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.565 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.580 |
LIG_GBD_Chelix_1 | 297 | 305 | PF00786 | 0.593 |
LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.717 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.477 |
LIG_NRBOX | 116 | 122 | PF00104 | 0.324 |
LIG_REV1ctd_RIR_1 | 172 | 181 | PF16727 | 0.436 |
LIG_RPA_C_Fungi | 360 | 372 | PF08784 | 0.432 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.421 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.505 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.505 |
LIG_SH2_SRC | 308 | 311 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 451 | 455 | PF00017 | 0.465 |
LIG_SH2_STAT3 | 505 | 508 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.428 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.230 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.425 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.588 |
LIG_SUMO_SIM_par_1 | 336 | 342 | PF11976 | 0.497 |
LIG_TYR_ITIM | 301 | 306 | PF00017 | 0.598 |
LIG_WRC_WIRS_1 | 171 | 176 | PF05994 | 0.424 |
MOD_CDK_SPxK_1 | 430 | 436 | PF00069 | 0.605 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.615 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.656 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.524 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.400 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.522 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.661 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.604 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.565 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.640 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.610 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.421 |
MOD_CMANNOS | 469 | 472 | PF00535 | 0.473 |
MOD_Cter_Amidation | 137 | 140 | PF01082 | 0.668 |
MOD_DYRK1A_RPxSP_1 | 354 | 358 | PF00069 | 0.630 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.574 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.600 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.609 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.420 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.468 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.680 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.324 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.647 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.492 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.594 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.614 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.495 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.342 |
MOD_LATS_1 | 363 | 369 | PF00433 | 0.582 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.684 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.183 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.468 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.550 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.656 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.588 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.511 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.338 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.520 |
MOD_NEK2_2 | 270 | 275 | PF00069 | 0.606 |
MOD_NEK2_2 | 312 | 317 | PF00069 | 0.484 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.599 |
MOD_NEK2_2 | 71 | 76 | PF00069 | 0.295 |
MOD_PIKK_1 | 504 | 510 | PF00454 | 0.382 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.603 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.653 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.371 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.501 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.473 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.528 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.568 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.577 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.638 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.489 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.692 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.593 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.610 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.419 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.324 |
TRG_DiLeu_BaEn_1 | 506 | 511 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.517 |
TRG_DiLeu_LyEn_5 | 506 | 511 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 501 | 506 | PF00026 | 0.596 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW11 | Leptomonas seymouri | 44% | 100% |
A0A3Q8IR86 | Leishmania donovani | 90% | 100% |
A4HPJ2 | Leishmania braziliensis | 77% | 100% |
A4ID71 | Leishmania infantum | 90% | 100% |
Q4Q193 | Leishmania major | 91% | 100% |