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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HC27
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 13 |
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018107 | peptidyl-threonine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0018210 | peptidyl-threonine modification | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004672 | protein kinase activity | 3 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0004713 | protein tyrosine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.622 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 263 | 271 | PF00400 | 0.404 |
DEG_APCC_DBOX_1 | 303 | 311 | PF00400 | 0.333 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.449 |
DOC_CYCLIN_RxL_1 | 49 | 59 | PF00134 | 0.486 |
DOC_CYCLIN_yCln2_LP_2 | 135 | 141 | PF00134 | 0.507 |
DOC_MAPK_FxFP_2 | 446 | 449 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 11 | 18 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 190 | 198 | PF00069 | 0.264 |
DOC_MAPK_gen_1 | 360 | 369 | PF00069 | 0.256 |
DOC_MAPK_HePTP_8 | 357 | 369 | PF00069 | 0.256 |
DOC_MAPK_MEF2A_6 | 190 | 198 | PF00069 | 0.264 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.256 |
DOC_MAPK_MEF2A_6 | 372 | 379 | PF00069 | 0.256 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.284 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 46 | 50 | PF12436 | 0.626 |
LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 224 | 230 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 304 | 313 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 471 | 477 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.747 |
LIG_Actin_WH2_2 | 295 | 313 | PF00022 | 0.404 |
LIG_Actin_WH2_2 | 465 | 483 | PF00022 | 0.410 |
LIG_APCC_ABBA_1 | 163 | 168 | PF00400 | 0.440 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.284 |
LIG_Clathr_ClatBox_1 | 395 | 399 | PF01394 | 0.346 |
LIG_Clathr_ClatBox_1 | 458 | 462 | PF01394 | 0.346 |
LIG_EH1_1 | 251 | 259 | PF00400 | 0.342 |
LIG_eIF4E_1 | 252 | 258 | PF01652 | 0.415 |
LIG_eIF4E_1 | 262 | 268 | PF01652 | 0.398 |
LIG_eIF4E_1 | 439 | 445 | PF01652 | 0.404 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.284 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.269 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.266 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.422 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.381 |
LIG_HCF-1_HBM_1 | 463 | 466 | PF13415 | 0.346 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.256 |
LIG_LIR_Gen_1 | 140 | 147 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 179 | 188 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.171 |
LIG_LIR_Gen_1 | 250 | 260 | PF02991 | 0.130 |
LIG_LIR_Gen_1 | 463 | 474 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 179 | 183 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.171 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 259 | 263 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.257 |
LIG_PCNA_yPIPBox_3 | 298 | 307 | PF02747 | 0.346 |
LIG_Rb_pABgroove_1 | 114 | 122 | PF01858 | 0.556 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.171 |
LIG_SH2_NCK_1 | 106 | 110 | PF00017 | 0.412 |
LIG_SH2_SRC | 106 | 109 | PF00017 | 0.413 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.368 |
LIG_SH2_SRC | 279 | 282 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.319 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.550 |
LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.284 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.443 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.304 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.364 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.476 |
LIG_SH3_5 | 118 | 122 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 265 | 272 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 315 | 320 | PF11976 | 0.171 |
LIG_SUMO_SIM_par_1 | 265 | 272 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 339 | 346 | PF11976 | 0.404 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.658 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.330 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.275 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.639 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.658 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.399 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.188 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.198 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.404 |
MOD_Cter_Amidation | 188 | 191 | PF01082 | 0.226 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.593 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.342 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.313 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.257 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.258 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.404 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.585 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.404 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.439 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.647 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.579 |
MOD_N-GLC_1 | 424 | 429 | PF02516 | 0.346 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.352 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.376 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.347 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.343 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.302 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.330 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.661 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.558 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.657 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.269 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.269 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.256 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.659 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.654 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.171 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.179 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.346 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.346 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.253 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.269 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.381 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.294 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.375 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.627 |
MOD_SUMO_for_1 | 176 | 179 | PF00179 | 0.305 |
MOD_SUMO_for_1 | 323 | 326 | PF00179 | 0.256 |
MOD_SUMO_rev_2 | 108 | 115 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 317 | 325 | PF00179 | 0.263 |
MOD_SUMO_rev_2 | 332 | 341 | PF00179 | 0.274 |
TRG_DiLeu_BaEn_1 | 265 | 270 | PF01217 | 0.346 |
TRG_DiLeu_BaEn_1 | 440 | 445 | PF01217 | 0.307 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.271 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.234 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.559 |
TRG_ER_diLys_1 | 495 | 499 | PF00400 | 0.291 |
TRG_NES_CRM1_1 | 265 | 276 | PF08389 | 0.210 |
TRG_NLS_MonoExtC_3 | 48 | 53 | PF00514 | 0.649 |
TRG_NLS_MonoExtN_4 | 46 | 53 | PF00514 | 0.714 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4D6 | Leptomonas seymouri | 33% | 69% |
A0A0N1IJ52 | Leptomonas seymouri | 64% | 99% |
A0A0N1PBM1 | Leptomonas seymouri | 32% | 68% |
A0A0S4IIU2 | Bodo saltans | 32% | 100% |
A0A0S4IVF2 | Bodo saltans | 25% | 100% |
A0A0S4IYY9 | Bodo saltans | 25% | 100% |
A0A0S4J2K6 | Bodo saltans | 31% | 100% |
A0A0S4J343 | Bodo saltans | 47% | 89% |
A0A0S4J8J4 | Bodo saltans | 26% | 100% |
A0A0S4JUY0 | Bodo saltans | 28% | 84% |
A0A0S4JZV2 | Bodo saltans | 26% | 100% |
A0A1X0NHA6 | Trypanosomatidae | 47% | 95% |
A0A1X0NMR5 | Trypanosomatidae | 25% | 100% |
A0A1X0NMS0 | Trypanosomatidae | 25% | 100% |
A0A1X0NQT9 | Trypanosomatidae | 26% | 100% |
A0A1X0P3K5 | Trypanosomatidae | 33% | 100% |
A0A3Q8IC55 | Leishmania donovani | 89% | 100% |
A0A3Q8IDK8 | Leishmania donovani | 24% | 89% |
A0A3R7KRM5 | Trypanosoma rangeli | 36% | 74% |
A0A3S5H6C8 | Leishmania donovani | 26% | 100% |
A0A3S5H7N7 | Leishmania donovani | 25% | 100% |
A0A3S7WQK7 | Leishmania donovani | 26% | 100% |
A0A3S7WR45 | Leishmania donovani | 28% | 100% |
A0A3S7X9D1 | Leishmania donovani | 31% | 87% |
A0A422N7C9 | Trypanosoma rangeli | 24% | 80% |
A0A422N878 | Trypanosoma rangeli | 47% | 95% |
A0A422P2B2 | Trypanosoma rangeli | 26% | 100% |
A3EZ55 | Wallemia ichthyophaga (strain EXF-994 / CBS 113033) | 26% | 100% |
A4H5L7 | Leishmania braziliensis | 26% | 100% |
A4H641 | Leishmania braziliensis | 28% | 100% |
A4H9D1 | Leishmania braziliensis | 28% | 100% |
A4HA94 | Leishmania braziliensis | 24% | 100% |
A4HG27 | Leishmania braziliensis | 24% | 92% |
A4HIM5 | Leishmania braziliensis | 25% | 100% |
A4HMK7 | Leishmania braziliensis | 31% | 87% |
A4HTV4 | Leishmania infantum | 26% | 100% |
A4HTV5 | Leishmania infantum | 26% | 100% |
A4HUG1 | Leishmania infantum | 28% | 100% |
A4HZH0 | Leishmania infantum | 89% | 100% |
A4I349 | Leishmania infantum | 24% | 88% |
A4I5X0 | Leishmania infantum | 25% | 100% |
A4IB86 | Leishmania infantum | 31% | 87% |
B0Y4X4 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 27% | 100% |
C9ZVD8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A105 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 97% |
E8NHK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AF07 | Leishmania major | 30% | 87% |
E9AMP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AN59 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AVG0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B663 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 87% |
G4N374 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 26% | 100% |
O13352 | Magnaporthe oryzae | 26% | 100% |
O35491 | Mus musculus | 26% | 100% |
O42099 | Cyprinus carpio | 29% | 100% |
O43781 | Homo sapiens | 32% | 85% |
O61443 | Drosophila melanogaster | 28% | 100% |
O80673 | Arabidopsis thaliana | 27% | 87% |
P27361 | Homo sapiens | 25% | 100% |
P40417 | Drosophila melanogaster | 27% | 100% |
P49760 | Homo sapiens | 27% | 100% |
P51566 | Arabidopsis thaliana | 27% | 100% |
P51567 | Arabidopsis thaliana | 27% | 100% |
P53779 | Homo sapiens | 27% | 100% |
Q10156 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 72% |
Q39011 | Arabidopsis thaliana | 24% | 100% |
Q39012 | Arabidopsis thaliana | 25% | 100% |
Q39023 | Arabidopsis thaliana | 25% | 100% |
Q40531 | Nicotiana tabacum | 25% | 100% |
Q4Q701 | Leishmania major | 26% | 100% |
Q4QC19 | Leishmania major | 88% | 100% |
Q4QFG6 | Leishmania major | 33% | 96% |
Q4QHG6 | Leishmania major | 28% | 100% |
Q4QHY3 | Leishmania major | 26% | 100% |
Q4QHY4 | Leishmania major | 26% | 100% |
Q4R6S5 | Macaca fascicularis | 32% | 88% |
Q4V8A3 | Rattus norvegicus | 29% | 85% |
Q4WQR3 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 100% |
Q501Q9 | Xenopus laevis | 24% | 85% |
Q5U4C9 | Mus musculus | 32% | 83% |
Q5VP69 | Oryza sativa subsp. japonica | 27% | 100% |
Q5ZIU3 | Gallus gallus | 32% | 95% |
Q84UI5 | Oryza sativa subsp. japonica | 26% | 100% |
Q8SQZ4 | Encephalitozoon cuniculi (strain GB-M1) | 30% | 100% |
Q90327 | Cyprinus carpio | 29% | 100% |
Q922Y0 | Mus musculus | 33% | 85% |
Q99078 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 100% |
Q9DGD9 | Danio rerio | 29% | 100% |
Q9P6P3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 93% |
Q9V3D5 | Drosophila melanogaster | 34% | 69% |
V5DIC3 | Trypanosoma cruzi | 47% | 83% |