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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005759 | mitochondrial matrix | 5 | 7 |
GO:0031974 | membrane-enclosed lumen | 2 | 7 |
GO:0043233 | organelle lumen | 3 | 7 |
GO:0070013 | intracellular organelle lumen | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
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: E9B5I3
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
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 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004740 | pyruvate dehydrogenase (acetyl-transferring) kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.608 |
CLV_C14_Caspase3-7 | 304 | 308 | PF00656 | 0.354 |
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.309 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.292 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.427 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.318 |
CLV_PCSK_PC7_1 | 253 | 259 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.304 |
DEG_APCC_DBOX_1 | 226 | 234 | PF00400 | 0.402 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.471 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.629 |
DEG_SPOP_SBC_1 | 334 | 338 | PF00917 | 0.445 |
DEG_SPOP_SBC_1 | 483 | 487 | PF00917 | 0.537 |
DOC_CKS1_1 | 26 | 31 | PF01111 | 0.379 |
DOC_CYCLIN_RxL_1 | 15 | 28 | PF00134 | 0.403 |
DOC_CYCLIN_RxL_1 | 185 | 194 | PF00134 | 0.608 |
DOC_CYCLIN_yCln2_LP_2 | 341 | 347 | PF00134 | 0.505 |
DOC_MAPK_FxFP_2 | 131 | 134 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 212 | 221 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 224 | 232 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 384 | 393 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 472 | 482 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 212 | 221 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 224 | 232 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 384 | 393 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 475 | 482 | PF00069 | 0.443 |
DOC_MAPK_NFAT4_5 | 214 | 222 | PF00069 | 0.465 |
DOC_PP1_RVXF_1 | 186 | 193 | PF00149 | 0.545 |
DOC_PP1_RVXF_1 | 255 | 262 | PF00149 | 0.336 |
DOC_PP1_RVXF_1 | 468 | 474 | PF00149 | 0.304 |
DOC_PP1_RVXF_1 | 80 | 86 | PF00149 | 0.403 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.398 |
DOC_PP2B_LxvP_1 | 30 | 33 | PF13499 | 0.355 |
DOC_PP2B_PxIxI_1 | 386 | 392 | PF00149 | 0.304 |
DOC_PP4_FxxP_1 | 131 | 134 | PF00568 | 0.556 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.430 |
DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.304 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.449 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 10 | 19 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 358 | 364 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 394 | 403 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.433 |
LIG_Actin_WH2_2 | 360 | 378 | PF00022 | 0.369 |
LIG_APCC_ABBA_1 | 314 | 319 | PF00400 | 0.489 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 398 | 406 | PF00928 | 0.304 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.409 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.412 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.465 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.304 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.304 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.304 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.604 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.513 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.373 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.335 |
LIG_GBD_Chelix_1 | 47 | 55 | PF00786 | 0.371 |
LIG_LIR_Apic_2 | 128 | 134 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 300 | 306 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 458 | 465 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 60 | 71 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 300 | 305 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 458 | 463 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.359 |
LIG_MYND_1 | 130 | 134 | PF01753 | 0.545 |
LIG_Pex14_1 | 250 | 254 | PF04695 | 0.344 |
LIG_Pex14_1 | 85 | 89 | PF04695 | 0.384 |
LIG_Pex14_2 | 4 | 8 | PF04695 | 0.602 |
LIG_Pex14_2 | 418 | 422 | PF04695 | 0.304 |
LIG_SH2_CRK | 460 | 464 | PF00017 | 0.284 |
LIG_SH2_NCK_1 | 146 | 150 | PF00017 | 0.593 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.559 |
LIG_SH2_STAP1 | 432 | 436 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.320 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.340 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.390 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.325 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.304 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.391 |
LIG_SUMO_SIM_anti_2 | 231 | 237 | PF11976 | 0.417 |
LIG_SUMO_SIM_anti_2 | 388 | 393 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 297 | 304 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 310 | 315 | PF11976 | 0.370 |
LIG_UBA3_1 | 132 | 138 | PF00899 | 0.431 |
LIG_UBA3_1 | 219 | 224 | PF00899 | 0.322 |
LIG_WRC_WIRS_1 | 63 | 68 | PF05994 | 0.446 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.345 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.665 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.658 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.370 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.411 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.528 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.284 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.584 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.604 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.468 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.585 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.530 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.583 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.609 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.403 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.573 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.450 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.283 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.348 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.516 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.368 |
MOD_N-GLC_2 | 377 | 379 | PF02516 | 0.369 |
MOD_N-GLC_2 | 95 | 97 | PF02516 | 0.354 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.440 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.383 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.657 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.313 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.298 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.545 |
MOD_NEK2_2 | 379 | 384 | PF00069 | 0.369 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.487 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.544 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.422 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.376 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.340 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.399 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.570 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.477 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.512 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.482 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.422 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.334 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.358 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.502 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.366 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.542 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.378 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.424 |
MOD_SUMO_rev_2 | 315 | 324 | PF00179 | 0.429 |
TRG_DiLeu_BaEn_3 | 319 | 325 | PF01217 | 0.368 |
TRG_DiLeu_BaLyEn_6 | 215 | 220 | PF01217 | 0.360 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 226 | 229 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 469 | 472 | PF00400 | 0.304 |
TRG_NLS_MonoExtC_3 | 72 | 77 | PF00514 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.343 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P768 | Leptomonas seymouri | 55% | 100% |
A0A3Q8III9 | Leishmania donovani | 90% | 98% |
A4HBB1 | Leishmania braziliensis | 81% | 100% |
A4IAF9 | Leishmania infantum | 90% | 98% |
Q4Q2F2 | Leishmania major | 91% | 100% |