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: A4HH72
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0006811 | monoatomic ion transport | 4 | 6 |
GO:0006817 | phosphate ion transport | 7 | 6 |
GO:0006820 | monoatomic anion transport | 5 | 6 |
GO:0015698 | inorganic anion transport | 6 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
GO:0009987 | cellular process | 1 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0035435 | phosphate ion transmembrane transport | 6 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098661 | inorganic anion transmembrane transport | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 6 |
GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 6 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 6 |
GO:0015293 | symporter activity | 5 | 6 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 6 |
GO:0022804 | active transmembrane transporter activity | 3 | 6 |
GO:0022857 | transmembrane transporter activity | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.440 |
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.420 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.229 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.191 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.191 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.191 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.334 |
DEG_SPOP_SBC_1 | 277 | 281 | PF00917 | 0.391 |
DOC_CKS1_1 | 387 | 392 | PF01111 | 0.417 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.325 |
DOC_CYCLIN_yCln2_LP_2 | 537 | 543 | PF00134 | 0.442 |
DOC_MAPK_DCC_7 | 417 | 425 | PF00069 | 0.391 |
DOC_MAPK_DCC_7 | 79 | 88 | PF00069 | 0.286 |
DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 413 | 420 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.242 |
DOC_MAPK_MEF2A_6 | 184 | 192 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 92 | 99 | PF00069 | 0.248 |
DOC_PP1_RVXF_1 | 527 | 534 | PF00149 | 0.391 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.325 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.442 |
DOC_PP4_FxxP_1 | 290 | 293 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.248 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.282 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 300 | 305 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 435 | 440 | PF00244 | 0.403 |
LIG_APCC_ABBA_1 | 509 | 514 | PF00400 | 0.391 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.276 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.191 |
LIG_BRCT_BRCA1_1 | 37 | 41 | PF00533 | 0.442 |
LIG_CtBP_PxDLS_1 | 653 | 657 | PF00389 | 0.242 |
LIG_DLG_GKlike_1 | 435 | 443 | PF00625 | 0.391 |
LIG_EVH1_1 | 386 | 390 | PF00568 | 0.391 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.242 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.276 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.280 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.281 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.487 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.481 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.483 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.331 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.396 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.407 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.364 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.296 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.269 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.265 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.391 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.276 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.242 |
LIG_GSK3_LRP6_1 | 341 | 346 | PF00069 | 0.391 |
LIG_IRF3_LxIS_1 | 691 | 696 | PF10401 | 0.277 |
LIG_LIR_Apic_2 | 113 | 119 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 289 | 293 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 138 | 149 | PF02991 | 0.199 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 573 | 583 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 594 | 604 | PF02991 | 0.248 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 641 | 650 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 678 | 687 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.199 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 678 | 682 | PF02991 | 0.442 |
LIG_NRBOX | 169 | 175 | PF00104 | 0.205 |
LIG_NRBOX | 197 | 203 | PF00104 | 0.338 |
LIG_PTB_Apo_2 | 284 | 291 | PF02174 | 0.387 |
LIG_REV1ctd_RIR_1 | 288 | 292 | PF16727 | 0.442 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.276 |
LIG_SH3_2 | 342 | 347 | PF14604 | 0.391 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.404 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.480 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.427 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.448 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.442 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.442 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.205 |
LIG_SUMO_SIM_anti_2 | 93 | 98 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 118 | 123 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.187 |
LIG_SUMO_SIM_par_1 | 434 | 440 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 507 | 516 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 624 | 629 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 652 | 657 | PF11976 | 0.242 |
LIG_SUMO_SIM_par_1 | 691 | 696 | PF11976 | 0.276 |
LIG_TYR_ITIM | 56 | 61 | PF00017 | 0.276 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.276 |
LIG_WRC_WIRS_1 | 559 | 564 | PF05994 | 0.276 |
LIG_WRC_WIRS_1 | 580 | 585 | PF05994 | 0.191 |
MOD_CDC14_SPxK_1 | 344 | 347 | PF00782 | 0.391 |
MOD_CDK_SPxK_1 | 341 | 347 | PF00069 | 0.391 |
MOD_CDK_SPxK_1 | 626 | 632 | PF00069 | 0.442 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.391 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.587 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.568 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.521 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.455 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.279 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.255 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.276 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.391 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.442 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.276 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.242 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.245 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.243 |
MOD_GlcNHglycan | 36 | 40 | PF01048 | 0.242 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.277 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.203 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.242 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.292 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.196 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.157 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.486 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.313 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.486 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.442 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.276 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.205 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.433 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.489 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.415 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.509 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.443 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.383 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.442 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.447 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.452 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.424 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.255 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.321 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.276 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.242 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.276 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.367 |
MOD_LATS_1 | 433 | 439 | PF00433 | 0.391 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.550 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.187 |
MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.290 |
MOD_N-GLC_1 | 440 | 445 | PF02516 | 0.228 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.442 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.276 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.338 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.474 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.297 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.344 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.486 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.448 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.445 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.191 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.313 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.328 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.314 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.297 |
MOD_NEK2_1 | 693 | 698 | PF00069 | 0.313 |
MOD_NEK2_2 | 111 | 116 | PF00069 | 0.199 |
MOD_NEK2_2 | 3 | 8 | PF00069 | 0.298 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.242 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.391 |
MOD_PIKK_1 | 592 | 598 | PF00454 | 0.242 |
MOD_PIKK_1 | 654 | 660 | PF00454 | 0.276 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.391 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.286 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.469 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.422 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.442 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.442 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.454 |
MOD_Plk_2-3 | 278 | 284 | PF00069 | 0.421 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.239 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.330 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.476 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.276 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.304 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.509 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.427 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.442 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.442 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.411 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.276 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.276 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.311 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.311 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.325 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.325 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.585 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.540 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.528 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.442 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.442 |
MOD_SUMO_rev_2 | 464 | 474 | PF00179 | 0.391 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.277 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8C5 | Leptomonas seymouri | 62% | 100% |
A0A3S7X2A5 | Leishmania donovani | 76% | 100% |
A4I4B8 | Leishmania infantum | 77% | 100% |
E9ADR7 | Leishmania major | 76% | 99% |
Q6NV12 | Danio rerio | 23% | 100% |