Transporters, Uncharacterized
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: A4HRG7
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 | 283 | 287 | PF00656 | 0.738 |
CLV_C14_Caspase3-7 | 63 | 67 | PF00656 | 0.405 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.405 |
DEG_COP1_1 | 359 | 368 | PF00400 | 0.405 |
DEG_MDM2_SWIB_1 | 495 | 503 | PF02201 | 0.346 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.535 |
DEG_SCF_FBW7_1 | 219 | 226 | PF00400 | 0.405 |
DEG_SPOP_SBC_1 | 287 | 291 | PF00917 | 0.639 |
DEG_SPOP_SBC_1 | 330 | 334 | PF00917 | 0.542 |
DOC_CDC14_PxL_1 | 362 | 370 | PF14671 | 0.405 |
DOC_MAPK_gen_1 | 46 | 55 | PF00069 | 0.637 |
DOC_MAPK_JIP1_4 | 204 | 210 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 116 | 123 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 346 | 353 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 423 | 431 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 46 | 55 | PF00069 | 0.602 |
DOC_MAPK_NFAT4_5 | 116 | 124 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 338 | 341 | PF13499 | 0.662 |
DOC_PP2B_LxvP_1 | 363 | 366 | PF13499 | 0.405 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.405 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.405 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.221 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.405 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 417 | 427 | PF00244 | 0.506 |
LIG_APCC_ABBA_1 | 368 | 373 | PF00400 | 0.346 |
LIG_BRCT_BRCA1_1 | 263 | 267 | PF00533 | 0.684 |
LIG_BRCT_BRCA1_1 | 373 | 377 | 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 | 503 | 507 | PF01394 | 0.344 |
LIG_CSL_BTD_1 | 363 | 366 | PF09270 | 0.405 |
LIG_deltaCOP1_diTrp_1 | 20 | 29 | PF00928 | 0.455 |
LIG_deltaCOP1_diTrp_1 | 496 | 505 | PF00928 | 0.346 |
LIG_EH_1 | 264 | 268 | PF12763 | 0.687 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.459 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.405 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.405 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.322 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.405 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.405 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.368 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.435 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.700 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.414 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.476 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.539 |
LIG_LIR_Apic_2 | 392 | 397 | PF02991 | 0.546 |
LIG_LIR_Apic_2 | 422 | 428 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 198 | 208 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 496 | 506 | PF02991 | 0.346 |
LIG_LIR_LC3C_4 | 405 | 410 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.346 |
LIG_MLH1_MIPbox_1 | 87 | 91 | PF16413 | 0.312 |
LIG_MYND_1 | 28 | 32 | PF01753 | 0.405 |
LIG_MYND_3 | 365 | 369 | PF01753 | 0.405 |
LIG_NRBOX | 407 | 413 | PF00104 | 0.356 |
LIG_NRBOX | 464 | 470 | PF00104 | 0.356 |
LIG_Pex14_1 | 452 | 456 | PF04695 | 0.651 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.356 |
LIG_Pex14_2 | 353 | 357 | PF04695 | 0.405 |
LIG_Pex14_2 | 377 | 381 | PF04695 | 0.405 |
LIG_Pex14_2 | 495 | 499 | PF04695 | 0.346 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.474 |
LIG_SH2_PTP2 | 237 | 240 | PF00017 | 0.272 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.638 |
LIG_SH2_SRC | 371 | 374 | PF00017 | 0.312 |
LIG_SH2_SRC | 425 | 428 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.598 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.332 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.516 |
LIG_SUMO_SIM_par_1 | 366 | 374 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 407 | 413 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 60 | 66 | PF11976 | 0.483 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.405 |
LIG_UBA3_1 | 465 | 470 | PF00899 | 0.405 |
LIG_WRC_WIRS_1 | 386 | 391 | PF05994 | 0.405 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.464 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.279 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.675 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.711 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.759 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.663 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.670 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.546 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.346 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.353 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.539 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.678 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.344 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.247 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.519 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.202 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.448 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.452 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.522 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.547 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.421 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.477 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.558 |
MOD_GlcNHglycan | 551 | 555 | PF01048 | 0.505 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.632 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.420 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.652 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.225 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.292 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.686 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.732 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.740 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.602 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.495 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.346 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.721 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.706 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.336 |
MOD_LATS_1 | 278 | 284 | PF00433 | 0.752 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.460 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.684 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.751 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.727 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.248 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.666 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.588 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.422 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.437 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.405 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.348 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.645 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.405 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.329 |
MOD_NEK2_2 | 14 | 19 | PF00069 | 0.441 |
MOD_NEK2_2 | 195 | 200 | PF00069 | 0.571 |
MOD_NEK2_2 | 331 | 336 | PF00069 | 0.671 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.405 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.435 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.649 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.660 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.621 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.485 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.346 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.303 |
MOD_Plk_2-3 | 545 | 551 | PF00069 | 0.643 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.473 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.535 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.586 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.319 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.678 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.329 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.392 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.405 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.346 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.511 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.230 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.405 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.384 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.405 |
MOD_SUMO_rev_2 | 173 | 182 | PF00179 | 0.712 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.405 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.312 |
TRG_PTS1 | 585 | 588 | PF00515 | 0.704 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H4V2 | Leishmania donovani | 99% | 100% |
A4H370 | Leishmania braziliensis | 72% | 100% |
E9AC35 | Leishmania major | 90% | 100% |
E9AJD1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |