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:0005759 | mitochondrial matrix | 5 | 9 |
GO:0031974 | membrane-enclosed lumen | 2 | 9 |
GO:0043233 | organelle lumen | 3 | 9 |
GO:0070013 | intracellular organelle lumen | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
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: A4HBB1
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
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 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004740 | pyruvate dehydrogenase (acetyl-transferring) kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.529 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 317 | 319 | PF00082 | 0.502 |
CLV_PCSK_PC7_1 | 248 | 254 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.433 |
CLV_Separin_Metazoa | 284 | 288 | PF03568 | 0.259 |
DEG_APCC_DBOX_1 | 223 | 231 | PF00400 | 0.403 |
DEG_SCF_FBW7_1 | 347 | 352 | PF00400 | 0.457 |
DEG_SPOP_SBC_1 | 329 | 333 | PF00917 | 0.464 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.384 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.576 |
DOC_MAPK_gen_1 | 207 | 216 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 222 | 230 | PF00069 | 0.325 |
DOC_MAPK_gen_1 | 379 | 388 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 467 | 477 | PF00069 | 0.434 |
DOC_MAPK_HePTP_8 | 204 | 216 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 207 | 216 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 224 | 232 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 379 | 388 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 470 | 477 | PF00069 | 0.415 |
DOC_MAPK_NFAT4_5 | 209 | 217 | PF00069 | 0.466 |
DOC_PP1_RVXF_1 | 250 | 257 | PF00149 | 0.319 |
DOC_PP1_RVXF_1 | 463 | 469 | PF00149 | 0.288 |
DOC_PP1_RVXF_1 | 75 | 81 | PF00149 | 0.485 |
DOC_PP2B_LxvP_1 | 18 | 21 | PF13499 | 0.475 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.229 |
DOC_PP2B_PxIxI_1 | 324 | 330 | PF00149 | 0.299 |
DOC_PP2B_PxIxI_1 | 381 | 387 | PF00149 | 0.382 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.489 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.487 |
DOC_USP7_MATH_2 | 143 | 149 | PF00917 | 0.492 |
DOC_USP7_UBL2_3 | 414 | 418 | PF12436 | 0.382 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 110 | 116 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 130 | 140 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 389 | 398 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.383 |
LIG_Actin_WH2_2 | 355 | 373 | PF00022 | 0.421 |
LIG_Actin_WH2_2 | 63 | 81 | PF00022 | 0.381 |
LIG_APCC_ABBA_1 | 309 | 314 | PF00400 | 0.449 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.551 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.509 |
LIG_deltaCOP1_diTrp_1 | 393 | 401 | PF00928 | 0.382 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.498 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.441 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.360 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.595 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.300 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.358 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.381 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.317 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.585 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.580 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.479 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.382 |
LIG_GBD_Chelix_1 | 42 | 50 | PF00786 | 0.452 |
LIG_LIR_Apic_2 | 60 | 64 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 295 | 301 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 393 | 404 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 453 | 460 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 55 | 66 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 453 | 458 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.365 |
LIG_NRBOX | 281 | 287 | PF00104 | 0.257 |
LIG_PCNA_yPIPBox_3 | 279 | 288 | PF02747 | 0.264 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.349 |
LIG_Pex14_1 | 80 | 84 | PF04695 | 0.461 |
LIG_Pex14_2 | 413 | 417 | PF04695 | 0.382 |
LIG_SH2_STAP1 | 427 | 431 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.203 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.387 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.412 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.331 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.398 |
LIG_SUMO_SIM_anti_2 | 225 | 232 | PF11976 | 0.499 |
LIG_SUMO_SIM_anti_2 | 280 | 287 | PF11976 | 0.364 |
LIG_SUMO_SIM_anti_2 | 383 | 388 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 291 | 299 | PF11976 | 0.406 |
LIG_WRC_WIRS_1 | 455 | 460 | PF05994 | 0.209 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.438 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.604 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.759 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.635 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.410 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.528 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.372 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.597 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.315 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.328 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.602 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.342 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.594 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.532 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.308 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.583 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.583 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.491 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.398 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.487 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.520 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.487 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.322 |
MOD_N-GLC_2 | 372 | 374 | PF02516 | 0.323 |
MOD_N-GLC_2 | 90 | 92 | PF02516 | 0.450 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.705 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.444 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.426 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.288 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.249 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.498 |
MOD_NEK2_2 | 374 | 379 | PF00069 | 0.360 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.451 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.328 |
MOD_PKA_1 | 208 | 214 | PF00069 | 0.386 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.416 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.646 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.406 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.420 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.639 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.331 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.360 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.377 |
MOD_Plk_2-3 | 135 | 141 | PF00069 | 0.414 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.565 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.566 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.548 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.607 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.410 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.428 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.459 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.454 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.379 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.308 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.630 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.531 |
MOD_SUMO_rev_2 | 314 | 319 | PF00179 | 0.405 |
TRG_DiLeu_BaEn_1 | 383 | 388 | PF01217 | 0.209 |
TRG_DiLeu_BaEn_3 | 314 | 320 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 221 | 224 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P768 | Leptomonas seymouri | 54% | 100% |
A0A1X0PBH1 | Trypanosomatidae | 36% | 100% |
A0A3Q8III9 | Leishmania donovani | 82% | 98% |
A0A3S5IRS7 | Trypanosoma rangeli | 35% | 100% |
A4IAF9 | Leishmania infantum | 82% | 98% |
E9B5I3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q2F2 | Leishmania major | 81% | 100% |