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: E9AND6
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 1 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.570 |
DEG_MDM2_SWIB_1 | 166 | 173 | PF02201 | 0.445 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.626 |
DOC_CYCLIN_yCln2_LP_2 | 159 | 165 | PF00134 | 0.411 |
DOC_MAPK_gen_1 | 95 | 105 | PF00069 | 0.253 |
DOC_MAPK_MEF2A_6 | 17 | 26 | PF00069 | 0.506 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.524 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.533 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.458 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.227 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.411 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.411 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.530 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.361 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.411 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.339 |
LIG_LIR_Apic_2 | 130 | 135 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 144 | 155 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 211 | 222 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 70 | 81 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.458 |
LIG_Pex14_2 | 166 | 170 | PF04695 | 0.483 |
LIG_PTB_Apo_2 | 193 | 200 | PF02174 | 0.411 |
LIG_PTB_Phospho_1 | 193 | 199 | PF10480 | 0.411 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.393 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.425 |
LIG_SH3_5 | 83 | 87 | PF00018 | 0.445 |
LIG_SUMO_SIM_anti_2 | 236 | 241 | PF11976 | 0.433 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.526 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.227 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.317 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.529 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.597 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.371 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.445 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.515 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.469 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.393 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.467 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.358 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.415 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.506 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.501 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.531 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.423 |
MOD_N-GLC_2 | 14 | 16 | PF02516 | 0.468 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.616 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.445 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.366 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.481 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.516 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.621 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.522 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.261 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.445 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.570 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.342 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.257 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.530 |
MOD_SUMO_rev_2 | 53 | 60 | PF00179 | 0.493 |
TRG_DiLeu_BaEn_3 | 144 | 150 | PF01217 | 0.227 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.505 |
TRG_ER_diLys_1 | 242 | 247 | PF00400 | 0.481 |
TRG_ER_FFAT_2 | 144 | 154 | PF00635 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.227 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDF1 | Leptomonas seymouri | 61% | 99% |
A0A3S7WRE9 | Leishmania donovani | 87% | 79% |
A4H6B4 | Leishmania braziliensis | 74% | 100% |
A4HUN7 | Leishmania infantum | 89% | 100% |
E9ACR1 | Leishmania major | 89% | 100% |