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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q9Q0
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0022607 | cellular component assembly | 4 | 7 |
GO:0043248 | proteasome assembly | 6 | 7 |
GO:0043933 | protein-containing complex organization | 4 | 7 |
GO:0065003 | protein-containing complex assembly | 5 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.311 |
CLV_PCSK_FUR_1 | 168 | 172 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.468 |
DEG_APCC_DBOX_1 | 175 | 183 | PF00400 | 0.310 |
DOC_CYCLIN_RxL_1 | 194 | 203 | PF00134 | 0.469 |
DOC_MAPK_FxFP_2 | 64 | 67 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 176 | 184 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 93 | 100 | PF00069 | 0.422 |
DOC_MAPK_NFAT4_5 | 93 | 101 | PF00069 | 0.425 |
DOC_PP1_RVXF_1 | 58 | 65 | PF00149 | 0.476 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 60 | 65 | PF00244 | 0.397 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.310 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.434 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.310 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.383 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.612 |
LIG_LIR_Apic_2 | 61 | 67 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 105 | 111 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 143 | 152 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 105 | 109 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.310 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 125 | 129 | PF00017 | 0.494 |
LIG_SH2_PTP2 | 106 | 109 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.509 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.470 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.576 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.551 |
LIG_TYR_ITIM | 104 | 109 | PF00017 | 0.366 |
LIG_UBA3_1 | 1 | 9 | PF00899 | 0.560 |
MOD_CDC14_SPxK_1 | 217 | 220 | PF00782 | 0.604 |
MOD_CDK_SPxK_1 | 214 | 220 | PF00069 | 0.575 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.297 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.562 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.604 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.470 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.423 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.368 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.310 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.713 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.595 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.532 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.385 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.560 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.499 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.310 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.410 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.231 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.645 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.481 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.340 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.500 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.611 |
MOD_PKB_1 | 58 | 66 | PF00069 | 0.439 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.447 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.310 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.534 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.320 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.434 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.412 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.575 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.637 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.719 |
TRG_DiLeu_LyEn_5 | 174 | 179 | PF01217 | 0.310 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W5 | Leptomonas seymouri | 65% | 100% |
A0A3Q8IGP4 | Leishmania donovani | 96% | 100% |
A4HE91 | Leishmania braziliensis | 75% | 88% |
A4I1N7 | Leishmania infantum | 96% | 100% |
E9AXS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |