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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: E9ALH5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 14 |
GO:0006793 | phosphorus metabolic process | 3 | 14 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 14 |
GO:0006807 | nitrogen compound metabolic process | 2 | 14 |
GO:0008152 | metabolic process | 1 | 14 |
GO:0009987 | cellular process | 1 | 14 |
GO:0016310 | phosphorylation | 5 | 14 |
GO:0019538 | protein metabolic process | 3 | 14 |
GO:0036211 | protein modification process | 4 | 14 |
GO:0043170 | macromolecule metabolic process | 3 | 14 |
GO:0043412 | macromolecule modification | 4 | 14 |
GO:0044237 | cellular metabolic process | 2 | 14 |
GO:0044238 | primary metabolic process | 2 | 14 |
GO:0071704 | organic substance metabolic process | 2 | 14 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003824 | catalytic activity | 1 | 14 |
GO:0004672 | protein kinase activity | 3 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0016301 | kinase activity | 4 | 14 |
GO:0016740 | transferase activity | 2 | 14 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 14 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 14 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.501 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.280 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.204 |
DOC_CKS1_1 | 11 | 16 | PF01111 | 0.253 |
DOC_CYCLIN_RxL_1 | 158 | 169 | PF00134 | 0.536 |
DOC_MAPK_gen_1 | 256 | 266 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 290 | 300 | PF00069 | 0.353 |
DOC_MAPK_gen_1 | 40 | 47 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 60 | 70 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 265 | 273 | PF00069 | 0.275 |
DOC_MAPK_MEF2A_6 | 315 | 323 | PF00069 | 0.160 |
DOC_MAPK_MEF2A_6 | 40 | 47 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 63 | 72 | PF00069 | 0.283 |
DOC_PP2B_LxvP_1 | 128 | 131 | PF13499 | 0.559 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.260 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.248 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.275 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.420 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.171 |
LIG_14-3-3_CanoR_1 | 258 | 266 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 40 | 44 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 403 | 413 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.591 |
LIG_APCC_ABBAyCdc20_2 | 193 | 199 | PF00400 | 0.429 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.533 |
LIG_BRCT_BRCA1_1 | 406 | 410 | PF00533 | 0.405 |
LIG_Clathr_ClatBox_1 | 308 | 312 | PF01394 | 0.275 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.394 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.256 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.387 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.339 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.273 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.462 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.424 |
LIG_FXI_DFP_1 | 364 | 368 | PF00024 | 0.324 |
LIG_GBD_Chelix_1 | 269 | 277 | PF00786 | 0.353 |
LIG_LIR_Apic_2 | 332 | 338 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 407 | 418 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 66 | 73 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.465 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.454 |
LIG_SH2_PTP2 | 67 | 70 | PF00017 | 0.301 |
LIG_SH2_SRC | 226 | 229 | PF00017 | 0.324 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.301 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.294 |
LIG_SH2_STAT3 | 433 | 436 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.210 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.331 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.707 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.324 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.405 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.340 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.329 |
LIG_SUMO_SIM_anti_2 | 188 | 194 | PF11976 | 0.405 |
LIG_SUMO_SIM_anti_2 | 295 | 301 | PF11976 | 0.275 |
LIG_SUMO_SIM_anti_2 | 303 | 310 | PF11976 | 0.275 |
LIG_SUMO_SIM_anti_2 | 320 | 325 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 315 | 320 | PF11976 | 0.226 |
LIG_SUMO_SIM_par_1 | 376 | 381 | PF11976 | 0.160 |
LIG_TYR_ITIM | 224 | 229 | PF00017 | 0.275 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.449 |
LIG_UBA3_1 | 377 | 384 | PF00899 | 0.160 |
LIG_WW_1 | 51 | 54 | PF00397 | 0.445 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.272 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.524 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.324 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.420 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.463 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.367 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.336 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.319 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.329 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.433 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.317 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.283 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.463 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.437 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.417 |
MOD_N-GLC_2 | 19 | 21 | PF02516 | 0.399 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.425 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.275 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.335 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.570 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.579 |
MOD_PK_1 | 265 | 271 | PF00069 | 0.275 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.375 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.281 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.304 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.425 |
MOD_PKB_1 | 214 | 222 | PF00069 | 0.234 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.379 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.324 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.172 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.286 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.374 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.253 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.275 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.319 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.434 |
MOD_SUMO_for_1 | 292 | 295 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 246 | 253 | PF00179 | 0.407 |
MOD_SUMO_rev_2 | 341 | 349 | PF00179 | 0.425 |
TRG_DiLeu_BaEn_1 | 295 | 300 | PF01217 | 0.298 |
TRG_DiLeu_BaEn_1 | 303 | 308 | PF01217 | 0.248 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.321 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.490 |
TRG_NES_CRM1_1 | 409 | 421 | PF08389 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT76 | Leptomonas seymouri | 73% | 100% |
A0A0N1HTF0 | Leptomonas seymouri | 24% | 71% |
A0A0N1IM47 | Leptomonas seymouri | 27% | 100% |
A0A0S4IXR9 | Bodo saltans | 27% | 97% |
A0A0S4IZ14 | Bodo saltans | 24% | 75% |
A0A0S4JWD5 | Bodo saltans | 28% | 100% |
A0A0S4KN74 | Bodo saltans | 27% | 100% |
A0A1X0PA19 | Trypanosomatidae | 46% | 90% |
A0A3Q8IAQ1 | Leishmania donovani | 26% | 100% |
A0A3Q8IDY1 | Leishmania donovani | 95% | 100% |
A0A3R7K1T4 | Trypanosoma rangeli | 47% | 89% |
A0A3R7M848 | Trypanosoma rangeli | 28% | 96% |
A0A3S7X2W9 | Leishmania donovani | 25% | 100% |
A0A3S7X7D5 | Leishmania donovani | 28% | 100% |
A0A422P3P9 | Trypanosoma rangeli | 27% | 90% |
A4HCE6 | Leishmania braziliensis | 25% | 100% |
A4HHP8 | Leishmania braziliensis | 81% | 100% |
A4HHS9 | Leishmania braziliensis | 25% | 100% |
A4HZW8 | Leishmania infantum | 26% | 100% |
A4I4W3 | Leishmania infantum | 95% | 100% |
A4I4Y0 | Leishmania infantum | 25% | 100% |
A4I9H1 | Leishmania infantum | 28% | 100% |
C9ZKZ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 95% |
C9ZW20 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 77% |
E9AEB1 | Leishmania major | 92% | 100% |
E9AJJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 83% |
E9ALF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B4G9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
F4IS56 | Arabidopsis thaliana | 23% | 94% |
Q2V419 | Arabidopsis thaliana | 26% | 100% |
Q3SYZ2 | Bos taurus | 27% | 100% |
Q4QBQ2 | Leishmania major | 27% | 100% |
Q66H84 | Rattus norvegicus | 28% | 100% |
Q7YRC6 | Bos taurus | 26% | 100% |
Q8LF80 | Arabidopsis thaliana | 26% | 100% |
Q9NI63 | Drosophila melanogaster | 27% | 84% |
V5BPJ0 | Trypanosoma cruzi | 26% | 91% |
V5BSK0 | Trypanosoma cruzi | 49% | 90% |