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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9AJD1
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 6 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 6 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 6 |
GO:0015098 | molybdate ion transmembrane transporter activity | 5 | 6 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 6 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 6 |
GO:0022857 | transmembrane transporter activity | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.732 |
CLV_C14_Caspase3-7 | 63 | 67 | PF00656 | 0.405 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.516 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 526 | 528 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.405 |
DEG_COP1_1 | 360 | 369 | PF00400 | 0.405 |
DEG_MDM2_SWIB_1 | 243 | 251 | PF02201 | 0.284 |
DEG_MDM2_SWIB_1 | 496 | 504 | PF02201 | 0.346 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.529 |
DEG_SCF_FBW7_1 | 221 | 228 | PF00400 | 0.405 |
DOC_CDC14_PxL_1 | 363 | 371 | PF14671 | 0.405 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.272 |
DOC_CYCLIN_yCln2_LP_2 | 30 | 36 | PF00134 | 0.362 |
DOC_MAPK_gen_1 | 115 | 123 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 46 | 55 | PF00069 | 0.642 |
DOC_MAPK_JIP1_4 | 206 | 212 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 115 | 123 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 347 | 354 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 424 | 432 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 46 | 55 | PF00069 | 0.607 |
DOC_MAPK_NFAT4_5 | 116 | 124 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 339 | 342 | PF13499 | 0.675 |
DOC_PP2B_LxvP_1 | 364 | 367 | PF13499 | 0.405 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.405 |
DOC_PP4_FxxP_1 | 395 | 398 | PF00568 | 0.405 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.221 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.405 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.541 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 418 | 428 | PF00244 | 0.515 |
LIG_APCC_ABBA_1 | 369 | 374 | PF00400 | 0.346 |
LIG_BRCT_BRCA1_1 | 374 | 378 | PF00533 | 0.346 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.405 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.221 |
LIG_Clathr_ClatBox_1 | 504 | 508 | PF01394 | 0.344 |
LIG_CSL_BTD_1 | 364 | 367 | PF09270 | 0.405 |
LIG_deltaCOP1_diTrp_1 | 20 | 29 | PF00928 | 0.464 |
LIG_deltaCOP1_diTrp_1 | 497 | 506 | PF00928 | 0.346 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.459 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.405 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.405 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.322 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.405 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.405 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.368 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.435 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.678 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.414 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.481 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.549 |
LIG_LIR_Apic_2 | 393 | 398 | PF02991 | 0.546 |
LIG_LIR_Apic_2 | 423 | 429 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 497 | 507 | PF02991 | 0.346 |
LIG_LIR_LC3C_4 | 406 | 411 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 497 | 503 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 568 | 574 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.223 |
LIG_MLH1_MIPbox_1 | 87 | 91 | PF16413 | 0.312 |
LIG_MYND_1 | 28 | 32 | PF01753 | 0.405 |
LIG_MYND_3 | 366 | 370 | PF01753 | 0.405 |
LIG_NRBOX | 408 | 414 | PF00104 | 0.356 |
LIG_NRBOX | 465 | 471 | PF00104 | 0.356 |
LIG_Pex14_1 | 453 | 457 | PF04695 | 0.674 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.356 |
LIG_Pex14_2 | 354 | 358 | PF04695 | 0.405 |
LIG_Pex14_2 | 378 | 382 | PF04695 | 0.405 |
LIG_Pex14_2 | 496 | 500 | PF04695 | 0.346 |
LIG_SH2_CRK | 426 | 430 | PF00017 | 0.481 |
LIG_SH2_NCK_1 | 328 | 332 | PF00017 | 0.528 |
LIG_SH2_SRC | 328 | 331 | PF00017 | 0.656 |
LIG_SH2_SRC | 372 | 375 | PF00017 | 0.312 |
LIG_SH2_SRC | 426 | 429 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 328 | 332 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.708 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.229 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.272 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.653 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.607 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.513 |
LIG_SUMO_SIM_anti_2 | 135 | 140 | PF11976 | 0.223 |
LIG_SUMO_SIM_anti_2 | 463 | 468 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 367 | 375 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 408 | 414 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 60 | 66 | PF11976 | 0.483 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.405 |
LIG_TYR_ITIM | 96 | 101 | PF00017 | 0.223 |
LIG_UBA3_1 | 466 | 471 | PF00899 | 0.405 |
LIG_WRC_WIRS_1 | 387 | 392 | PF05994 | 0.405 |
MOD_CDC14_SPxK_1 | 320 | 323 | PF00782 | 0.600 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.603 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.464 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.284 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.724 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.384 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.753 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.639 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.685 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.546 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.346 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.524 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.353 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.545 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.676 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.344 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.599 |
MOD_Cter_Amidation | 524 | 527 | PF01082 | 0.454 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.507 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.284 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.202 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.449 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.465 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.517 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.523 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.450 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.540 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.421 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.501 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.553 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.629 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.420 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.663 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.225 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.292 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.738 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.732 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.619 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.495 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.346 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.737 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.712 |
MOD_LATS_1 | 279 | 285 | PF00433 | 0.748 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.680 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.731 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.248 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.697 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.350 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.422 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.437 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.405 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.405 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.321 |
MOD_NEK2_2 | 14 | 19 | PF00069 | 0.444 |
MOD_NEK2_2 | 332 | 337 | PF00069 | 0.687 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.405 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.435 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.494 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.216 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.625 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.481 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.346 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.303 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.477 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.540 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.607 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.319 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.392 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.405 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.346 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.553 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.230 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.405 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.405 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.541 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.223 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 347 | 351 | PF00026 | 0.312 |
TRG_PTS1 | 579 | 582 | PF00515 | 0.689 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H4V2 | Leishmania donovani | 86% | 99% |
A4H370 | Leishmania braziliensis | 71% | 100% |
A4HRG7 | Leishmania infantum | 86% | 99% |
E9AC35 | Leishmania major | 84% | 100% |