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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QI26
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 122 | 128 | PF00089 | 0.346 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.529 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.346 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.772 |
DOC_CYCLIN_yCln2_LP_2 | 32 | 38 | PF00134 | 0.772 |
DOC_PP2B_LxvP_1 | 51 | 54 | PF13499 | 0.637 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.755 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 177 | 187 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 206 | 215 | PF00244 | 0.769 |
LIG_BRCT_BRCA1_1 | 194 | 198 | PF00533 | 0.782 |
LIG_BRCT_MDC1_1 | 294 | 298 | PF00533 | 0.685 |
LIG_deltaCOP1_diTrp_1 | 14 | 17 | PF00928 | 0.757 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.766 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.756 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.514 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.683 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.672 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.631 |
LIG_Integrin_isoDGR_2 | 268 | 270 | PF01839 | 0.682 |
LIG_LIR_Gen_1 | 14 | 24 | PF02991 | 0.760 |
LIG_LIR_Gen_1 | 2 | 13 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 278 | 288 | PF02991 | 0.749 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.762 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.753 |
LIG_PTAP_UEV_1 | 20 | 25 | PF05743 | 0.760 |
LIG_PTAP_UEV_1 | 247 | 252 | PF05743 | 0.676 |
LIG_PTB_Apo_2 | 227 | 234 | PF02174 | 0.694 |
LIG_PTB_Phospho_1 | 227 | 233 | PF10480 | 0.696 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.546 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.649 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.780 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.685 |
LIG_SH3_2 | 21 | 26 | PF14604 | 0.760 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.708 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.751 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.607 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.711 |
LIG_SH3_5 | 71 | 75 | PF00018 | 0.742 |
LIG_TYR_ITIM | 279 | 284 | PF00017 | 0.652 |
MOD_CDC14_SPxK_1 | 80 | 83 | PF00782 | 0.658 |
MOD_CDK_SPxK_1 | 77 | 83 | PF00069 | 0.662 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.630 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.701 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.717 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.655 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.590 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.600 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.614 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.607 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.782 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.346 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.624 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.626 |
MOD_GlcNHglycan | 200 | 204 | PF01048 | 0.590 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.656 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.665 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.578 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.692 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.633 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.734 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.687 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.725 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.676 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.662 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.679 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.691 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.610 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.724 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.802 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.661 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.658 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.557 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.734 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.623 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.766 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.757 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.629 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.746 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.616 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.727 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.711 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.548 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.712 |
MOD_Plk_2-3 | 112 | 118 | PF00069 | 0.546 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.725 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.659 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.760 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.626 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.666 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.662 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.650 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2F1 | Leptomonas seymouri | 50% | 96% |
A0A3S7WQG5 | Leishmania donovani | 95% | 100% |
A4H5I6 | Leishmania braziliensis | 86% | 100% |
A4HTS7 | Leishmania infantum | 95% | 100% |
E9AML0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |