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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0016020 | membrane | 2 | 7 |
Related structures:
AlphaFold database: Q4QBP6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 9 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006820 | monoatomic anion transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 9 |
GO:0015711 | organic anion transport | 5 | 2 |
GO:0015780 | nucleotide-sugar transmembrane transport | 3 | 2 |
GO:0015931 | nucleobase-containing compound transport | 5 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0051179 | localization | 1 | 9 |
GO:0051234 | establishment of localization | 2 | 9 |
GO:0055085 | transmembrane transport | 2 | 9 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072334 | UDP-galactose transmembrane transport | 5 | 2 |
GO:0090481 | pyrimidine nucleotide-sugar transmembrane transport | 4 | 2 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 2 |
GO:1901264 | carbohydrate derivative transport | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 2 |
GO:0005459 | UDP-galactose transmembrane transporter activity | 6 | 2 |
GO:0005460 | UDP-glucose transmembrane transporter activity | 6 | 2 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 2 |
GO:0008514 | organic anion transmembrane transporter activity | 5 | 2 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 2 |
GO:0015165 | pyrimidine nucleotide-sugar transmembrane transporter activity | 5 | 2 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.734 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.734 |
CLV_PCSK_PC1ET2_1 | 317 | 319 | PF00082 | 0.277 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.537 |
DEG_APCC_DBOX_1 | 328 | 336 | PF00400 | 0.468 |
DEG_SCF_FBW7_1 | 16 | 22 | PF00400 | 0.592 |
DEG_SPOP_SBC_1 | 263 | 267 | PF00917 | 0.305 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.251 |
DEG_SPOP_SBC_1 | 517 | 521 | PF00917 | 0.755 |
DOC_CKS1_1 | 16 | 21 | PF01111 | 0.708 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 327 | 336 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 210 | 220 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 232 | 240 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 317 | 326 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 452 | 459 | PF00069 | 0.275 |
DOC_MAPK_HePTP_8 | 207 | 219 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 210 | 219 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 320 | 328 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 452 | 461 | PF00069 | 0.275 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.260 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.502 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.763 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 140 | 144 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 389 | 398 | PF00244 | 0.205 |
LIG_Actin_WH2_2 | 125 | 142 | PF00022 | 0.309 |
LIG_Actin_WH2_2 | 436 | 454 | PF00022 | 0.331 |
LIG_Actin_WH2_2 | 482 | 499 | PF00022 | 0.488 |
LIG_APCC_ABBA_1 | 396 | 401 | PF00400 | 0.288 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.745 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.572 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.389 |
LIG_Clathr_ClatBox_1 | 342 | 346 | PF01394 | 0.364 |
LIG_deltaCOP1_diTrp_1 | 349 | 358 | PF00928 | 0.333 |
LIG_EVH1_1 | 16 | 20 | PF00568 | 0.667 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.747 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.377 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.325 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.340 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.460 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.293 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.344 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.478 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.614 |
LIG_GBD_Chelix_1 | 38 | 46 | PF00786 | 0.350 |
LIG_LIR_Gen_1 | 192 | 203 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 403 | 413 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 470 | 481 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 486 | 496 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.440 |
LIG_NRBOX | 298 | 304 | PF00104 | 0.389 |
LIG_NRBOX | 420 | 426 | PF00104 | 0.466 |
LIG_Pex14_1 | 354 | 358 | PF04695 | 0.333 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.499 |
LIG_RPA_C_Fungi | 84 | 96 | PF08784 | 0.456 |
LIG_SH2_CRK | 534 | 538 | PF00017 | 0.552 |
LIG_SH2_GRB2like | 307 | 310 | PF00017 | 0.396 |
LIG_SH2_GRB2like | 488 | 491 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 534 | 538 | PF00017 | 0.591 |
LIG_SH2_PTP2 | 488 | 491 | PF00017 | 0.496 |
LIG_SH2_SRC | 488 | 491 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.565 |
LIG_SH3_1 | 14 | 20 | PF00018 | 0.610 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.700 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.665 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.715 |
LIG_SUMO_SIM_anti_2 | 32 | 39 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 202 | 208 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 296 | 301 | PF11976 | 0.233 |
LIG_SUMO_SIM_par_1 | 343 | 349 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 441 | 446 | PF11976 | 0.355 |
LIG_TRAF2_1 | 507 | 510 | PF00917 | 0.545 |
LIG_ULM_U2AF65_1 | 317 | 322 | PF00076 | 0.405 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.412 |
LIG_WW_3 | 18 | 22 | PF00397 | 0.476 |
MOD_CDC14_SPxK_1 | 572 | 575 | PF00782 | 0.709 |
MOD_CDK_SPxK_1 | 15 | 21 | PF00069 | 0.603 |
MOD_CDK_SPxK_1 | 569 | 575 | PF00069 | 0.709 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.652 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.365 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.335 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.380 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.390 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.357 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.412 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.684 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.676 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.391 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.648 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.326 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.190 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.376 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.412 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.280 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.417 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.671 |
MOD_GlcNHglycan | 546 | 550 | PF01048 | 0.680 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.490 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.447 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.410 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.721 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.317 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.279 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.284 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.351 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.350 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.374 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.237 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.327 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.331 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.714 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.776 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.586 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.636 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.410 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.331 |
MOD_N-GLC_1 | 526 | 531 | PF02516 | 0.695 |
MOD_N-GLC_2 | 167 | 169 | PF02516 | 0.594 |
MOD_N-GLC_2 | 49 | 51 | PF02516 | 0.412 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.438 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.557 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.364 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.349 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.438 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.343 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.366 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.361 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.350 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.364 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.574 |
MOD_NEK2_2 | 110 | 115 | PF00069 | 0.526 |
MOD_NEK2_2 | 53 | 58 | PF00069 | 0.379 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.466 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.331 |
MOD_PK_1 | 453 | 459 | PF00069 | 0.364 |
MOD_PKA_1 | 199 | 205 | PF00069 | 0.412 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.633 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.490 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.386 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.233 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.255 |
MOD_PKB_1 | 387 | 395 | PF00069 | 0.233 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.466 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.525 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.428 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.587 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.572 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.412 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.382 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.371 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.345 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.294 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.303 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.348 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.331 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.331 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.620 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.648 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.738 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.738 |
MOD_SUMO_for_1 | 57 | 60 | PF00179 | 0.372 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.709 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.466 |
TRG_ER_diLys_1 | 575 | 580 | PF00400 | 0.796 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7F6 | Leptomonas seymouri | 50% | 100% |
A0A1X0NV21 | Trypanosomatidae | 38% | 100% |
A0A3Q8IBG5 | Leishmania donovani | 88% | 99% |
A0A422N3L8 | Trypanosoma rangeli | 36% | 100% |
A4HCB7 | Leishmania braziliensis | 69% | 100% |
A4HZX4 | Leishmania infantum | 88% | 99% |
E9AVT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
P0CP32 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 26% | 100% |
P0CP33 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 26% | 100% |