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:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005743 | mitochondrial inner membrane | 5 | 3 |
GO:0019866 | organelle inner membrane | 4 | 3 |
GO:0031090 | organelle membrane | 3 | 3 |
GO:0031966 | mitochondrial membrane | 4 | 3 |
Related structures:
AlphaFold database: A4H7Q3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0006811 | monoatomic ion transport | 4 | 3 |
GO:0006820 | monoatomic anion transport | 5 | 3 |
GO:0006862 | nucleotide transport | 6 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0015711 | organic anion transport | 5 | 3 |
GO:0015748 | organophosphate ester transport | 5 | 3 |
GO:0015865 | purine nucleotide transport | 7 | 3 |
GO:0015866 | ADP transport | 6 | 3 |
GO:0015867 | ATP transport | 6 | 3 |
GO:0015868 | purine ribonucleotide transport | 6 | 3 |
GO:0015931 | nucleobase-containing compound transport | 5 | 3 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0051503 | adenine nucleotide transport | 8 | 3 |
GO:0055085 | transmembrane transport | 2 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0071705 | nitrogen compound transport | 4 | 3 |
GO:0072530 | purine-containing compound transmembrane transport | 3 | 3 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 3 |
GO:0140021 | mitochondrial ADP transmembrane transport | 4 | 3 |
GO:1901264 | carbohydrate derivative transport | 5 | 3 |
GO:1901679 | nucleotide transmembrane transport | 3 | 3 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 3 |
GO:1990544 | mitochondrial ATP transmembrane transport | 4 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000295 | adenine nucleotide transmembrane transporter activity | 6 | 3 |
GO:0005215 | transporter activity | 1 | 3 |
GO:0005346 | purine ribonucleotide transmembrane transporter activity | 4 | 3 |
GO:0005347 | ATP transmembrane transporter activity | 5 | 3 |
GO:0005471 | ATP:ADP antiporter activity | 5 | 3 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 3 |
GO:0008514 | organic anion transmembrane transporter activity | 5 | 3 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 3 |
GO:0015215 | nucleotide transmembrane transporter activity | 4 | 3 |
GO:0015216 | purine nucleotide transmembrane transporter activity | 5 | 3 |
GO:0015217 | ADP transmembrane transporter activity | 5 | 3 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 3 |
GO:0015297 | antiporter activity | 5 | 3 |
GO:0015605 | organophosphate ester transmembrane transporter activity | 3 | 3 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 3 |
GO:0022804 | active transmembrane transporter activity | 3 | 3 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:0140323 | obsolete solute:monoatomic anion antiporter activity | 6 | 3 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.349 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.513 |
CLV_PCSK_PC7_1 | 173 | 179 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.408 |
DEG_APCC_DBOX_1 | 324 | 332 | PF00400 | 0.411 |
DOC_CDC14_PxL_1 | 203 | 211 | PF14671 | 0.240 |
DOC_CYCLIN_yCln2_LP_2 | 122 | 128 | PF00134 | 0.566 |
DOC_CYCLIN_yCln2_LP_2 | 352 | 358 | PF00134 | 0.593 |
DOC_CYCLIN_yCln2_LP_2 | 365 | 371 | PF00134 | 0.654 |
DOC_MAPK_gen_1 | 149 | 157 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 177 | 184 | PF00069 | 0.332 |
DOC_MAPK_gen_1 | 219 | 227 | PF00069 | 0.629 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.674 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 127 | 131 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 200 | 206 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 219 | 229 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 258 | 266 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 290 | 295 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 37 | 44 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 58 | 62 | PF00244 | 0.726 |
LIG_Actin_WH2_2 | 206 | 221 | PF00022 | 0.489 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.705 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.511 |
LIG_Clathr_ClatBox_1 | 88 | 92 | PF01394 | 0.630 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.333 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.558 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.682 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.492 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.670 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.614 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.366 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.465 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.724 |
LIG_GBD_Chelix_1 | 168 | 176 | PF00786 | 0.450 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 432 | 436 | PF02991 | 0.429 |
LIG_LYPXL_yS_3 | 436 | 439 | PF13949 | 0.349 |
LIG_PCNA_yPIPBox_3 | 267 | 279 | PF02747 | 0.501 |
LIG_RPA_C_Fungi | 330 | 342 | PF08784 | 0.240 |
LIG_SH2_CRK | 310 | 314 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 10 | 14 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.490 |
LIG_SH2_SRC | 10 | 13 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.240 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.688 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.591 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.668 |
LIG_SUMO_SIM_anti_2 | 65 | 72 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 180 | 185 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 207 | 212 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 65 | 72 | PF11976 | 0.491 |
LIG_UBA3_1 | 328 | 333 | PF00899 | 0.405 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.490 |
LIG_WRC_WIRS_1 | 430 | 435 | PF05994 | 0.526 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.453 |
MOD_CDC14_SPxK_1 | 19 | 22 | PF00782 | 0.508 |
MOD_CDK_SPxK_1 | 16 | 22 | PF00069 | 0.510 |
MOD_CDK_SPxxK_3 | 117 | 124 | PF00069 | 0.720 |
MOD_CDK_SPxxK_3 | 16 | 23 | PF00069 | 0.511 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.538 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.622 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.279 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.629 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.478 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.513 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.436 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.497 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.717 |
MOD_GlcNHglycan | 140 | 145 | PF01048 | 0.593 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.490 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.529 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.683 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.491 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.697 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.395 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.450 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.619 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.622 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.510 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.376 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.498 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.526 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.399 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.334 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.588 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.534 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.357 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.712 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.391 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.528 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.542 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.613 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.291 |
MOD_NEK2_2 | 320 | 325 | PF00069 | 0.413 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.524 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.693 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.424 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.240 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.485 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.448 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.693 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.352 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.618 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.693 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.384 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.406 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.476 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.453 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.492 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.555 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.763 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.641 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.240 |
TRG_DiLeu_BaEn_4 | 34 | 40 | PF01217 | 0.664 |
TRG_DiLeu_BaLyEn_6 | 425 | 430 | PF01217 | 0.568 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.423 |
TRG_ER_diArg_1 | 21 | 23 | PF00400 | 0.769 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 329 | 332 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.425 |
TRG_NLS_MonoExtN_4 | 330 | 336 | PF00514 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 37 | 41 | PF00026 | 0.654 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD69 | Leptomonas seymouri | 25% | 100% |
A0A1X0NP33 | Trypanosomatidae | 24% | 100% |
A0A3Q8I9V0 | Leishmania donovani | 72% | 100% |
A4HW42 | Leishmania infantum | 71% | 100% |
C9ZSY0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9APU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QFN5 | Leishmania major | 72% | 100% |