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:0005759 | mitochondrial matrix | 5 | 8 |
GO:0031974 | membrane-enclosed lumen | 2 | 8 |
GO:0043233 | organelle lumen | 3 | 8 |
GO:0070013 | intracellular organelle lumen | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8III9
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0006109 | regulation of carbohydrate metabolic process | 5 | 1 |
GO:0006468 | protein phosphorylation | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0010675 | obsolete regulation of cellular carbohydrate metabolic process | 5 | 1 |
GO:0010906 | regulation of glucose metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0062012 | regulation of small molecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004672 | protein kinase activity | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0004740 | pyruvate dehydrogenase (acetyl-transferring) kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 143 | 147 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.414 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.555 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.477 |
CLV_PCSK_PC7_1 | 257 | 263 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.430 |
DEG_SCF_FBW7_1 | 356 | 361 | PF00400 | 0.567 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.735 |
DEG_SPOP_SBC_1 | 338 | 342 | PF00917 | 0.611 |
DEG_SPOP_SBC_1 | 487 | 491 | PF00917 | 0.623 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 189 | 198 | PF00134 | 0.712 |
DOC_CYCLIN_yCln2_LP_2 | 345 | 351 | PF00134 | 0.688 |
DOC_MAPK_gen_1 | 216 | 225 | PF00069 | 0.625 |
DOC_MAPK_gen_1 | 388 | 397 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 476 | 486 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.625 |
DOC_MAPK_MEF2A_6 | 388 | 397 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 479 | 486 | PF00069 | 0.469 |
DOC_MAPK_NFAT4_5 | 218 | 226 | PF00069 | 0.603 |
DOC_PP1_RVXF_1 | 259 | 266 | PF00149 | 0.411 |
DOC_PP1_RVXF_1 | 472 | 478 | PF00149 | 0.366 |
DOC_PP1_RVXF_1 | 84 | 90 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 27 | 30 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.487 |
DOC_PP2B_PxIxI_1 | 390 | 396 | PF00149 | 0.430 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.515 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.567 |
DOC_USP7_UBL2_3 | 423 | 427 | PF12436 | 0.390 |
DOC_USP7_UBL2_3 | 77 | 81 | PF12436 | 0.552 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 139 | 149 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 216 | 222 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 231 | 237 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 362 | 368 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 398 | 407 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 65 | 71 | PF00244 | 0.507 |
LIG_Actin_WH2_2 | 364 | 382 | PF00022 | 0.460 |
LIG_APCC_ABBA_1 | 318 | 323 | PF00400 | 0.564 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.682 |
LIG_deltaCOP1_diTrp_1 | 402 | 410 | PF00928 | 0.430 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.538 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.480 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.429 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.617 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.385 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.316 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.430 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.287 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.768 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.657 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.503 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.430 |
LIG_GBD_Chelix_1 | 51 | 59 | PF00786 | 0.490 |
LIG_LIR_Apic_2 | 69 | 73 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 304 | 310 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 402 | 411 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 462 | 469 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.711 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.783 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.437 |
LIG_MYND_1 | 134 | 138 | PF01753 | 0.653 |
LIG_Pex14_1 | 254 | 258 | PF04695 | 0.420 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.506 |
LIG_Pex14_2 | 422 | 426 | PF04695 | 0.430 |
LIG_Pex14_2 | 8 | 12 | PF04695 | 0.686 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.706 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.699 |
LIG_SH2_STAP1 | 436 | 440 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.511 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.413 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.461 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.496 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.410 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.376 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.458 |
LIG_SUMO_SIM_anti_2 | 235 | 241 | PF11976 | 0.561 |
LIG_SUMO_SIM_anti_2 | 286 | 296 | PF11976 | 0.519 |
LIG_SUMO_SIM_anti_2 | 392 | 397 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 301 | 308 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 314 | 319 | PF11976 | 0.464 |
LIG_TYR_ITIM | 148 | 153 | PF00017 | 0.570 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.649 |
LIG_WRC_WIRS_1 | 67 | 72 | PF05994 | 0.579 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.641 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.788 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.727 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.426 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.499 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.591 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.507 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.522 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.670 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.410 |
MOD_GlcNHglycan | 118 | 122 | PF01048 | 0.534 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.705 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.735 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.575 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.697 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.581 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.680 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.525 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.533 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.522 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.646 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.560 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.497 |
MOD_N-GLC_2 | 381 | 383 | PF02516 | 0.430 |
MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.489 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.560 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.483 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.376 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.747 |
MOD_NEK2_2 | 383 | 388 | PF00069 | 0.501 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.543 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.665 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.468 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.720 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.649 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.387 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.501 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.695 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.599 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.599 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.528 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.456 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.466 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.462 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.487 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.619 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.458 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.653 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.537 |
MOD_SUMO_rev_2 | 319 | 328 | PF00179 | 0.558 |
TRG_DiLeu_BaEn_3 | 323 | 329 | PF01217 | 0.500 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.446 |
TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 106 | 110 | PF00026 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P768 | Leptomonas seymouri | 57% | 100% |
A0A1X0PBH1 | Trypanosomatidae | 37% | 100% |
A4HBB1 | Leishmania braziliensis | 82% | 100% |
A4IAF9 | Leishmania infantum | 100% | 100% |
E9B5I3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q2F2 | Leishmania major | 91% | 100% |