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. | yes | yes: 5 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ART5
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 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:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.587 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.477 |
CLV_Separin_Metazoa | 181 | 185 | PF03568 | 0.677 |
DEG_APCC_DBOX_1 | 183 | 191 | PF00400 | 0.677 |
DEG_SPOP_SBC_1 | 104 | 108 | PF00917 | 0.677 |
DOC_ANK_TNKS_1 | 14 | 21 | PF00023 | 0.677 |
DOC_CYCLIN_RxL_1 | 323 | 332 | PF00134 | 0.677 |
DOC_MAPK_gen_1 | 302 | 311 | PF00069 | 0.677 |
DOC_MAPK_MEF2A_6 | 235 | 244 | PF00069 | 0.677 |
DOC_MAPK_MEF2A_6 | 305 | 313 | PF00069 | 0.677 |
DOC_MAPK_MEF2A_6 | 346 | 355 | PF00069 | 0.726 |
DOC_MAPK_MEF2A_6 | 422 | 430 | PF00069 | 0.477 |
DOC_PP1_RVXF_1 | 51 | 58 | PF00149 | 0.677 |
DOC_PP2B_LxvP_1 | 290 | 293 | PF13499 | 0.677 |
DOC_PP4_FxxP_1 | 289 | 292 | PF00568 | 0.677 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.853 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.888 |
DOC_USP7_UBL2_3 | 114 | 118 | PF12436 | 0.677 |
DOC_USP7_UBL2_3 | 274 | 278 | PF12436 | 0.677 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.894 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.884 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.811 |
LIG_14-3-3_CanoR_1 | 217 | 223 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 54 | 60 | PF00244 | 0.677 |
LIG_Actin_WH2_2 | 38 | 55 | PF00022 | 0.677 |
LIG_APCC_ABBA_1 | 468 | 473 | PF00400 | 0.879 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.677 |
LIG_EH1_1 | 238 | 246 | PF00400 | 0.677 |
LIG_EH1_1 | 87 | 95 | PF00400 | 0.677 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.677 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.677 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.677 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.427 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.677 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.565 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.547 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.677 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.677 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.578 |
LIG_IRF3_LxIS_1 | 351 | 356 | PF10401 | 0.723 |
LIG_LIR_Apic_2 | 288 | 292 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 349 | 360 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.724 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.810 |
LIG_NBox_RRM_1 | 82 | 92 | PF00076 | 0.677 |
LIG_PAM2_1 | 55 | 67 | PF00658 | 0.677 |
LIG_PCNA_PIPBox_1 | 283 | 292 | PF02747 | 0.677 |
LIG_PCNA_yPIPBox_3 | 344 | 354 | PF02747 | 0.729 |
LIG_Pex14_1 | 427 | 431 | PF04695 | 0.577 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.726 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.677 |
LIG_REV1ctd_RIR_1 | 28 | 37 | PF16727 | 0.677 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.723 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.878 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.677 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.677 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.677 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.867 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.696 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.677 |
LIG_SH3_4 | 485 | 492 | PF00018 | 0.892 |
LIG_SUMO_SIM_anti_2 | 253 | 260 | PF11976 | 0.677 |
LIG_SUMO_SIM_par_1 | 106 | 113 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 253 | 260 | PF11976 | 0.677 |
LIG_SUMO_SIM_par_1 | 90 | 96 | PF11976 | 0.677 |
LIG_SUMO_SIM_par_1 | 97 | 102 | PF11976 | 0.590 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.677 |
LIG_TRAF2_1 | 517 | 520 | PF00917 | 0.883 |
LIG_UBA3_1 | 350 | 354 | PF00899 | 0.645 |
LIG_WRC_WIRS_1 | 286 | 291 | PF05994 | 0.577 |
LIG_WRC_WIRS_1 | 79 | 84 | PF05994 | 0.577 |
LIG_WW_3 | 181 | 185 | PF00397 | 0.577 |
LIG_WW_3 | 291 | 295 | PF00397 | 0.577 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.577 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.675 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.577 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.818 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.862 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.661 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.577 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.718 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.868 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.650 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.578 |
MOD_GlcNHglycan | 461 | 465 | PF01048 | 0.821 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.859 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.577 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.577 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.577 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.577 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.577 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.577 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.639 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.577 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.874 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.871 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.577 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.577 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.577 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.626 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.482 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.577 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.871 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.577 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.315 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.577 |
MOD_PK_1 | 268 | 274 | PF00069 | 0.577 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.577 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.577 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.876 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.577 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.227 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.577 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.577 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.577 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.651 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.419 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.577 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.688 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.868 |
MOD_SUMO_rev_2 | 161 | 169 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 291 | 300 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 304 | 314 | PF00179 | 0.350 |
TRG_DiLeu_BaEn_4 | 161 | 167 | PF01217 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.692 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.577 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 327 | 332 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
P05425 | Enterococcus hirae (strain ATCC 9790 / DSM 20160 / JCM 8729 / LMG 6399 / NBRC 3181 / NCIMB 6459 / NCDO 1258 / NCTC 12367 / WDCM 00089 / R) | 22% | 72% |