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: A0A3Q8ICR6
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_MEL_PAP_1 | 176 | 182 | PF00089 | 0.559 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.422 |
CLV_PCSK_PC7_1 | 254 | 260 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.442 |
CLV_Separin_Metazoa | 388 | 392 | PF03568 | 0.474 |
DEG_APCC_DBOX_1 | 342 | 350 | PF00400 | 0.399 |
DEG_APCC_DBOX_1 | 390 | 398 | PF00400 | 0.514 |
DOC_AGCK_PIF_1 | 180 | 185 | PF00069 | 0.606 |
DOC_CYCLIN_yCln2_LP_2 | 126 | 132 | PF00134 | 0.530 |
DOC_MAPK_DCC_7 | 16 | 24 | PF00069 | 0.568 |
DOC_MAPK_FxFP_2 | 60 | 63 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 100 | 106 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 222 | 231 | PF00069 | 0.447 |
DOC_PP1_RVXF_1 | 18 | 25 | PF00149 | 0.602 |
DOC_PP4_FxxP_1 | 60 | 63 | PF00568 | 0.526 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.483 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.230 |
LIG_14-3-3_CanoR_1 | 20 | 25 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 203 | 209 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 258 | 262 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 423 | 429 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 441 | 445 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 49 | 57 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 88 | 97 | PF00244 | 0.494 |
LIG_Actin_WH2_2 | 159 | 175 | PF00022 | 0.530 |
LIG_APCC_ABBA_1 | 330 | 335 | PF00400 | 0.514 |
LIG_APCC_Cbox_1 | 253 | 259 | PF00515 | 0.480 |
LIG_APCC_Cbox_2 | 253 | 259 | PF00515 | 0.408 |
LIG_Clathr_ClatBox_1 | 197 | 201 | PF01394 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 281 | 291 | PF00928 | 0.408 |
LIG_DLG_GKlike_1 | 267 | 274 | PF00625 | 0.447 |
LIG_EH1_1 | 268 | 276 | PF00400 | 0.447 |
LIG_eIF4E_1 | 269 | 275 | PF01652 | 0.480 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.547 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.506 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.444 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.314 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.483 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.449 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.401 |
LIG_LIR_Apic_2 | 58 | 63 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.388 |
LIG_LYPXL_SIV_4 | 244 | 252 | PF13949 | 0.434 |
LIG_LYPXL_yS_3 | 190 | 193 | PF13949 | 0.529 |
LIG_MYND_1 | 285 | 289 | PF01753 | 0.447 |
LIG_PCNA_PIPBox_1 | 28 | 37 | PF02747 | 0.537 |
LIG_PCNA_PIPBox_1 | 342 | 351 | PF02747 | 0.487 |
LIG_PTB_Apo_2 | 44 | 51 | PF02174 | 0.480 |
LIG_PTB_Phospho_1 | 44 | 50 | PF10480 | 0.488 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.469 |
LIG_SH2_NCK_1 | 269 | 273 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 418 | 422 | PF00017 | 0.515 |
LIG_SH2_SRC | 348 | 351 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.459 |
LIG_SH2_STAT3 | 358 | 361 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.527 |
LIG_SH3_2 | 386 | 391 | PF14604 | 0.460 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.589 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.530 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.503 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 109 | 115 | PF11976 | 0.538 |
LIG_SUMO_SIM_anti_2 | 160 | 167 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 164 | 170 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 238 | 243 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 91 | 99 | PF11976 | 0.512 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.519 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.434 |
LIG_TRAF2_1 | 305 | 308 | PF00917 | 0.447 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.591 |
LIG_TYR_ITIM | 396 | 401 | PF00017 | 0.458 |
LIG_UBA3_1 | 113 | 119 | PF00899 | 0.528 |
LIG_UBA3_1 | 197 | 205 | PF00899 | 0.264 |
MOD_CDK_SPK_2 | 258 | 263 | PF00069 | 0.480 |
MOD_CDK_SPxxK_3 | 336 | 343 | PF00069 | 0.522 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.487 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.480 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.628 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.424 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.236 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.415 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.434 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.736 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.538 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.696 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.496 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.544 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.543 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.533 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.586 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.622 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.554 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.343 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.355 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.451 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.469 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.582 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.382 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.464 |
MOD_NEK2_2 | 436 | 441 | PF00069 | 0.580 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.533 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.386 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.454 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.607 |
MOD_PKB_1 | 82 | 90 | PF00069 | 0.606 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.505 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.432 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.524 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.512 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.468 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.480 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.480 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.511 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.549 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.234 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.607 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.362 |
TRG_DiLeu_BaEn_1 | 341 | 346 | PF01217 | 0.473 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 154 | 157 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 221 | 224 | PF00400 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 136 | 141 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 343 | 347 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 37 | 41 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q6 | Leptomonas seymouri | 79% | 90% |
A0A0S4JSJ6 | Bodo saltans | 24% | 90% |
A0A422NVH3 | Trypanosoma rangeli | 34% | 96% |
A4HEP0 | Leishmania braziliensis | 91% | 100% |
A4I1W9 | Leishmania infantum | 100% | 100% |
C9ZS50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 96% |
E9AY15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4Q9F8 | Leishmania major | 95% | 100% |
V5BQ13 | Trypanosoma cruzi | 33% | 97% |