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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005743 | mitochondrial inner membrane | 5 | 2 |
GO:0019866 | organelle inner membrane | 4 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031966 | mitochondrial membrane | 4 | 2 |
Related structures:
AlphaFold database: A4HW42
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006820 | monoatomic anion transport | 5 | 2 |
GO:0006862 | nucleotide transport | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015711 | organic anion transport | 5 | 2 |
GO:0015748 | organophosphate ester transport | 5 | 2 |
GO:0015865 | purine nucleotide transport | 7 | 2 |
GO:0015866 | ADP transport | 6 | 2 |
GO:0015867 | ATP transport | 6 | 2 |
GO:0015868 | purine ribonucleotide transport | 6 | 2 |
GO:0015931 | nucleobase-containing compound transport | 5 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051503 | adenine nucleotide transport | 8 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072530 | purine-containing compound transmembrane transport | 3 | 2 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 2 |
GO:0140021 | mitochondrial ADP transmembrane transport | 4 | 2 |
GO:1901264 | carbohydrate derivative transport | 5 | 2 |
GO:1901679 | nucleotide transmembrane transport | 3 | 2 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 2 |
GO:1990544 | mitochondrial ATP transmembrane transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000295 | adenine nucleotide transmembrane transporter activity | 6 | 2 |
GO:0005215 | transporter activity | 1 | 2 |
GO:0005346 | purine ribonucleotide transmembrane transporter activity | 4 | 2 |
GO:0005347 | ATP transmembrane transporter activity | 5 | 2 |
GO:0005471 | ATP:ADP antiporter activity | 5 | 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:0015215 | nucleotide transmembrane transporter activity | 4 | 2 |
GO:0015216 | purine nucleotide transmembrane transporter activity | 5 | 2 |
GO:0015217 | ADP transmembrane transporter activity | 5 | 2 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 2 |
GO:0015297 | antiporter activity | 5 | 2 |
GO:0015605 | organophosphate ester transmembrane transporter activity | 3 | 2 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 2 |
GO:0022804 | active transmembrane transporter activity | 3 | 2 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0140323 | obsolete solute:monoatomic anion antiporter activity | 6 | 2 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.430 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.419 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.604 |
DEG_SPOP_SBC_1 | 43 | 47 | PF00917 | 0.633 |
DOC_CYCLIN_yCln2_LP_2 | 203 | 209 | PF00134 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.598 |
DOC_MAPK_gen_1 | 208 | 216 | PF00069 | 0.645 |
DOC_MAPK_gen_1 | 344 | 352 | PF00069 | 0.597 |
DOC_MAPK_MEF2A_6 | 319 | 327 | PF00069 | 0.455 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.733 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.769 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.808 |
LIG_14-3-3_CanoR_1 | 112 | 120 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 208 | 218 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 242 | 250 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 26 | 33 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 274 | 279 | PF00244 | 0.662 |
LIG_Actin_WH2_2 | 195 | 210 | PF00022 | 0.497 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.751 |
LIG_Clathr_ClatBox_1 | 77 | 81 | PF01394 | 0.650 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.555 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.501 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.676 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.729 |
LIG_Integrin_RGD_1 | 13 | 15 | PF01839 | 0.455 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.677 |
LIG_NRBOX | 322 | 328 | PF00104 | 0.424 |
LIG_PCNA_yPIPBox_3 | 390 | 398 | PF02747 | 0.608 |
LIG_PTAP_UEV_1 | 420 | 425 | PF05743 | 0.487 |
LIG_SH2_GRB2like | 378 | 381 | PF00017 | 0.607 |
LIG_SH2_NCK_1 | 243 | 247 | PF00017 | 0.652 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.641 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.763 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.684 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.538 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.492 |
LIG_WW_3 | 109 | 113 | PF00397 | 0.640 |
MOD_CDC14_SPxK_1 | 109 | 112 | PF00782 | 0.645 |
MOD_CDK_SPxK_1 | 106 | 112 | PF00069 | 0.649 |
MOD_CDK_SPxxK_3 | 106 | 113 | PF00069 | 0.771 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.600 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.423 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.544 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.736 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.492 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.433 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.615 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.532 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.495 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.456 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.385 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.431 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.698 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.481 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.749 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.612 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.474 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.440 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.629 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.326 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.720 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.656 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.401 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.350 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.655 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.711 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.687 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.220 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.376 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.410 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.657 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.396 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.611 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.728 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.727 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.646 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.648 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.657 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.728 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.683 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.660 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.433 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.292 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.432 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.375 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.501 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.619 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.802 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.685 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.764 |
TRG_DiLeu_BaEn_4 | 23 | 29 | PF01217 | 0.709 |
TRG_DiLeu_BaLyEn_6 | 409 | 414 | PF01217 | 0.557 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.796 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 343 | 346 | PF00400 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 124 | 129 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 162 | 166 | PF00026 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NP33 | Trypanosomatidae | 24% | 100% |
A0A3Q8I9V0 | Leishmania donovani | 98% | 99% |
A4H7Q3 | Leishmania braziliensis | 71% | 100% |
C9ZSY0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9APU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QFN5 | Leishmania major | 89% | 100% |