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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A4HJG4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016310 | phosphorylation | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004672 | protein kinase activity | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 414 | 418 | PF00656 | 0.549 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.779 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.826 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.826 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.757 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.673 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.549 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.819 |
DEG_SPOP_SBC_1 | 465 | 469 | PF00917 | 0.808 |
DOC_CKS1_1 | 342 | 347 | PF01111 | 0.549 |
DOC_CYCLIN_RxL_1 | 155 | 164 | PF00134 | 0.660 |
DOC_CYCLIN_RxL_1 | 214 | 221 | PF00134 | 0.549 |
DOC_CYCLIN_RxL_1 | 426 | 437 | PF00134 | 0.549 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 226 | 235 | PF00134 | 0.549 |
DOC_MAPK_DCC_7 | 40 | 48 | PF00069 | 0.784 |
DOC_MAPK_FxFP_2 | 262 | 265 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 263 | 272 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 40 | 48 | PF00069 | 0.784 |
DOC_MAPK_MEF2A_6 | 227 | 235 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 402 | 409 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.549 |
DOC_PP1_RVXF_1 | 27 | 33 | PF00149 | 0.710 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.762 |
DOC_PP4_FxxP_1 | 262 | 265 | PF00568 | 0.549 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.793 |
DOC_USP7_UBL2_3 | 388 | 392 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.375 |
LIG_14-3-3_CanoR_1 | 31 | 37 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 396 | 413 | PF00022 | 0.549 |
LIG_APCC_ABBAyCdc20_2 | 68 | 74 | PF00400 | 0.859 |
LIG_CtBP_PxDLS_1 | 92 | 98 | PF00389 | 0.851 |
LIG_deltaCOP1_diTrp_1 | 363 | 368 | PF00928 | 0.549 |
LIG_EH1_1 | 421 | 429 | PF00400 | 0.549 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.549 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.742 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.392 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.549 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.549 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.392 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.549 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.546 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.429 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.650 |
LIG_GBD_Chelix_1 | 423 | 431 | PF00786 | 0.549 |
LIG_Integrin_RGD_1 | 144 | 146 | PF01839 | 0.763 |
LIG_LIR_Apic_2 | 259 | 265 | PF02991 | 0.549 |
LIG_LIR_Apic_2 | 330 | 335 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.789 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.616 |
LIG_LYPXL_yS_3 | 264 | 267 | PF13949 | 0.549 |
LIG_SH2_PTP2 | 332 | 335 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 419 | 423 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 326 | 329 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.758 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.444 |
LIG_SH3_1 | 188 | 194 | PF00018 | 0.759 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.734 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.759 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.642 |
LIG_TRAF2_1 | 210 | 213 | PF00917 | 0.671 |
LIG_TRAF2_1 | 458 | 461 | PF00917 | 0.746 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.863 |
LIG_TYR_ITIM | 174 | 179 | PF00017 | 0.672 |
MOD_CDK_SPK_2 | 331 | 336 | PF00069 | 0.549 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.549 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.810 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.844 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.675 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.549 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.392 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.549 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.549 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.549 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.543 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.420 |
MOD_DYRK1A_RPxSP_1 | 200 | 204 | PF00069 | 0.712 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.661 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.712 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.549 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.357 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.549 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.803 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.789 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.743 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.549 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.549 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.549 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.549 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.827 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.549 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.746 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.549 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.802 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.824 |
MOD_NEK2_2 | 115 | 120 | PF00069 | 0.792 |
MOD_NEK2_2 | 253 | 258 | PF00069 | 0.549 |
MOD_OFUCOSY | 365 | 371 | PF10250 | 0.549 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.549 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.734 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.549 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.549 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.543 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.478 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.711 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.277 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.549 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.549 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.549 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.746 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.708 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.549 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.549 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.375 |
MOD_SUMO_rev_2 | 315 | 321 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 49 | 58 | PF00179 | 0.812 |
TRG_DiLeu_BaEn_1 | 382 | 387 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.689 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.823 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.772 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.866 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 429 | 434 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A2XW02 | ORYSI | 22% | 100% |
G4N7X0 | MAGO7 | 26% | 52% |
O14019 | SCHPO | 25% | 75% |
O59790 | SCHPO | 28% | 100% |
O88866 | MOUSE | 24% | 67% |
P28829 | SCHPO | 23% | 72% |
P32577 | RAT | 26% | 100% |
P41239 | CHICK | 26% | 100% |
P41240 | HUMAN | 26% | 100% |
P41241 | MOUSE | 27% | 100% |
P57058 | HUMAN | 24% | 67% |
Q54QI2 | DICDI | 31% | 50% |
Q55CE0 | DICDI | 31% | 70% |
Q68UT7 | PANTR | 24% | 67% |
Q7XR88 | ORYSJ | 22% | 100% |
Q86ME2 | CAEEL | 24% | 81% |
Q9STF0 | ARATH | 28% | 100% |