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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0000307 | cyclin-dependent protein kinase holoenzyme complex | 7 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005813 | centrosome | 3 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 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 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902554 | serine/threonine protein kinase complex | 6 | 1 |
GO:1902911 | protein kinase complex | 5 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HEP0
Term | Name | Level | Count |
---|---|---|---|
GO:0000079 | regulation of cyclin-dependent protein serine/threonine kinase activity | 6 | 1 |
GO:0001932 | regulation of protein phosphorylation | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0042325 | regulation of phosphorylation | 7 | 1 |
GO:0043549 | regulation of kinase activity | 5 | 1 |
GO:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0045859 | regulation of protein kinase activity | 6 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0071900 | regulation of protein serine/threonine kinase activity | 7 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
GO:1904029 | regulation of cyclin-dependent protein kinase activity | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016538 | cyclin-dependent protein serine/threonine kinase regulator activity | 5 | 1 |
GO:0019207 | kinase regulator activity | 3 | 1 |
GO:0019887 | protein kinase regulator activity | 4 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.517 |
CLV_MEL_PAP_1 | 166 | 172 | PF00089 | 0.550 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.341 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.428 |
CLV_PCSK_PC7_1 | 244 | 250 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.617 |
CLV_Separin_Metazoa | 299 | 303 | PF03568 | 0.266 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.498 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.480 |
DOC_AGCK_PIF_1 | 170 | 175 | PF00069 | 0.593 |
DOC_CYCLIN_RxL_1 | 299 | 308 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.517 |
DOC_MAPK_DCC_7 | 6 | 14 | PF00069 | 0.571 |
DOC_MAPK_FxFP_2 | 50 | 53 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 212 | 221 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 90 | 96 | PF00069 | 0.515 |
DOC_PP1_RVXF_1 | 300 | 307 | PF00149 | 0.383 |
DOC_PP1_RVXF_1 | 8 | 15 | PF00149 | 0.596 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.516 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.509 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.550 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 257 | 262 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 39 | 47 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 431 | 435 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 78 | 87 | PF00244 | 0.484 |
LIG_Actin_WH2_2 | 149 | 165 | PF00022 | 0.523 |
LIG_APCC_ABBA_1 | 320 | 325 | PF00400 | 0.505 |
LIG_APCC_Cbox_1 | 243 | 249 | PF00515 | 0.480 |
LIG_APCC_Cbox_2 | 243 | 249 | PF00515 | 0.408 |
LIG_Clathr_ClatBox_1 | 187 | 191 | PF01394 | 0.500 |
LIG_deltaCOP1_diTrp_1 | 138 | 143 | PF00928 | 0.321 |
LIG_deltaCOP1_diTrp_1 | 271 | 281 | PF00928 | 0.447 |
LIG_DLG_GKlike_1 | 257 | 264 | PF00625 | 0.447 |
LIG_EH1_1 | 258 | 266 | PF00400 | 0.447 |
LIG_eIF4E_1 | 259 | 265 | PF01652 | 0.480 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.466 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.519 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.430 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.301 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.464 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.453 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.449 |
LIG_LIR_Apic_2 | 48 | 53 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 233 | 242 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 278 | 289 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.419 |
LIG_LYPXL_yS_3 | 180 | 183 | PF13949 | 0.504 |
LIG_MYND_1 | 275 | 279 | PF01753 | 0.447 |
LIG_PCNA_PIPBox_1 | 18 | 27 | PF02747 | 0.526 |
LIG_PCNA_PIPBox_1 | 332 | 341 | PF02747 | 0.479 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.474 |
LIG_SH2_NCK_1 | 408 | 412 | PF00017 | 0.504 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.432 |
LIG_SH2_STAT3 | 348 | 351 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.516 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.524 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.568 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.516 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.473 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.517 |
LIG_SUMO_SIM_anti_2 | 108 | 114 | PF11976 | 0.369 |
LIG_SUMO_SIM_anti_2 | 99 | 105 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 228 | 233 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 81 | 89 | PF11976 | 0.496 |
LIG_SxIP_EBH_1 | 413 | 425 | PF03271 | 0.327 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.454 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.447 |
LIG_TYR_ITIM | 178 | 183 | PF00017 | 0.308 |
LIG_UBA3_1 | 103 | 109 | PF00899 | 0.518 |
MOD_CDK_SPK_2 | 248 | 253 | PF00069 | 0.480 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.356 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.480 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.457 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.615 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.620 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.379 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.430 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.414 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.505 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.684 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.496 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.513 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.549 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.544 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.517 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.608 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.620 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.475 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.500 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.340 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.376 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.457 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.490 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.379 |
MOD_NEK2_2 | 341 | 346 | PF00069 | 0.462 |
MOD_NEK2_2 | 376 | 381 | PF00069 | 0.428 |
MOD_NEK2_2 | 426 | 431 | PF00069 | 0.560 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.549 |
MOD_PKA_1 | 78 | 84 | PF00069 | 0.523 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.411 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.447 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.639 |
MOD_PKB_1 | 72 | 80 | PF00069 | 0.602 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.447 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.495 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.470 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.535 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.463 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.329 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.514 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.493 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.523 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.547 |
MOD_SUMO_for_1 | 252 | 255 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 28 | 37 | PF00179 | 0.391 |
TRG_DiLeu_BaEn_1 | 108 | 113 | PF01217 | 0.264 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.503 |
TRG_DiLeu_LyEn_5 | 331 | 336 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 126 | 131 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 15 | 19 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 302 | 307 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 78 | 82 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q6 | Leptomonas seymouri | 79% | 88% |
A0A0S4JSJ6 | Bodo saltans | 24% | 88% |
A0A3Q8ICR6 | Leishmania donovani | 91% | 98% |
A0A422NVH3 | Trypanosoma rangeli | 33% | 94% |
A4I1W9 | Leishmania infantum | 91% | 98% |
C9ZS50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 93% |
E9AY15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 98% |
Q4Q9F8 | Leishmania major | 90% | 100% |
V5BQ13 | Trypanosoma cruzi | 32% | 94% |