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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4IAA6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.581 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.498 |
CLV_Separin_Metazoa | 167 | 171 | PF03568 | 0.706 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.618 |
DOC_ANK_TNKS_1 | 182 | 189 | PF00023 | 0.626 |
DOC_MAPK_gen_1 | 176 | 184 | PF00069 | 0.621 |
DOC_PP2B_LxvP_1 | 311 | 314 | PF13499 | 0.758 |
DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.601 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.620 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 129 | 137 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 151 | 158 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 20 | 29 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 261 | 269 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 92 | 99 | PF00244 | 0.391 |
LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.535 |
LIG_APCC_ABBA_1 | 312 | 317 | PF00400 | 0.562 |
LIG_deltaCOP1_diTrp_1 | 148 | 152 | PF00928 | 0.491 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.642 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.530 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.598 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.306 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.512 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.674 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.366 |
LIG_Integrin_isoDGR_2 | 87 | 89 | PF01839 | 0.509 |
LIG_LIR_Apic_2 | 189 | 195 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.183 |
LIG_LIR_Gen_1 | 199 | 209 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 43 | 51 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 63 | 72 | PF02991 | 0.206 |
LIG_LIR_Gen_1 | 80 | 86 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.183 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.464 |
LIG_NRBOX | 204 | 210 | PF00104 | 0.455 |
LIG_REV1ctd_RIR_1 | 99 | 108 | PF16727 | 0.388 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.405 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.352 |
LIG_SH2_GRB2like | 109 | 112 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 82 | 86 | PF00017 | 0.352 |
LIG_SH3_2 | 165 | 170 | PF14604 | 0.601 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.600 |
LIG_SUMO_SIM_anti_2 | 203 | 211 | PF11976 | 0.524 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.564 |
LIG_TRFH_1 | 82 | 86 | PF08558 | 0.352 |
MOD_CDK_SPK_2 | 122 | 127 | PF00069 | 0.552 |
MOD_CDK_SPxxK_3 | 122 | 129 | PF00069 | 0.550 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.654 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.448 |
MOD_CMANNOS | 149 | 152 | PF00535 | 0.487 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.642 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.713 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.769 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.578 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.653 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.597 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.776 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.355 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.363 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.579 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.530 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.585 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.312 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.639 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.465 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.638 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.388 |
MOD_PK_1 | 214 | 220 | PF00069 | 0.642 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.579 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.525 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.537 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.581 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.619 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.312 |
MOD_PKB_1 | 127 | 135 | PF00069 | 0.561 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.618 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.607 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.331 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.262 |
MOD_Plk_2-3 | 143 | 149 | PF00069 | 0.476 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.684 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.582 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.602 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.654 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.595 |
TRG_NES_CRM1_1 | 66 | 79 | PF08389 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYK9 | Leptomonas seymouri | 49% | 97% |
A0A3Q8INP3 | Leishmania donovani | 100% | 100% |
A4HB59 | Leishmania braziliensis | 82% | 100% |
E9B5C9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q2K4 | Leishmania major | 93% | 100% |