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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3S5H5U9
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016701 | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen | 3 | 12 |
GO:0016702 | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen | 4 | 12 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0051213 | dioxygenase activity | 3 | 12 |
GO:0047800 | cysteamine dioxygenase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.539 |
CLV_PCSK_FUR_1 | 21 | 25 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 19 | 25 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.363 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.457 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.552 |
DOC_CYCLIN_RxL_1 | 126 | 135 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 253 | 259 | PF00134 | 0.440 |
DOC_PP1_RVXF_1 | 4 | 11 | PF00149 | 0.476 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.448 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.552 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.380 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.491 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.561 |
LIG_14-3-3_CanoR_1 | 12 | 22 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 86 | 96 | PF00244 | 0.584 |
LIG_BIR_III_2 | 187 | 191 | PF00653 | 0.457 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.570 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.591 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.491 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.532 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.552 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.361 |
LIG_LIR_Gen_1 | 41 | 51 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 50 | 54 | PF02991 | 0.529 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 230 | 234 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.462 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.493 |
LIG_TRFH_1 | 123 | 127 | PF08558 | 0.400 |
LIG_WRC_WIRS_1 | 40 | 45 | PF05994 | 0.480 |
MOD_CDC14_SPxK_1 | 3 | 6 | PF00782 | 0.462 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.396 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.497 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.306 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.420 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.453 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.362 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.418 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.649 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.388 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.454 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.398 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.308 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.444 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.350 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.335 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.386 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.487 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.432 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.381 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.289 |
MOD_NEK2_2 | 14 | 19 | PF00069 | 0.476 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.356 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.302 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.374 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.289 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.291 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.370 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.381 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.630 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.447 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.324 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.358 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C5 | Leptomonas seymouri | 57% | 100% |
A0A0S4IQ52 | Bodo saltans | 27% | 100% |
A0A1X0NH28 | Trypanosomatidae | 40% | 100% |
A0A422NM88 | Trypanosoma rangeli | 33% | 100% |
A4H4T5 | Leishmania braziliensis | 81% | 100% |
A4HT14 | Leishmania infantum | 99% | 100% |
C9ZTQ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AL02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QIV3 | Leishmania major | 92% | 100% |
V5BT74 | Trypanosoma cruzi | 38% | 100% |