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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HCS0
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 8 |
GO:0005509 | calcium ion binding | 5 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.674 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.801 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.542 |
CLV_Separin_Metazoa | 72 | 76 | PF03568 | 0.617 |
DEG_COP1_1 | 223 | 232 | PF00400 | 0.410 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.578 |
DOC_CDC14_PxL_1 | 197 | 205 | PF14671 | 0.546 |
DOC_MAPK_MEF2A_6 | 42 | 51 | PF00069 | 0.555 |
DOC_PP2B_PxIxI_1 | 172 | 178 | PF00149 | 0.490 |
DOC_PP2B_PxIxI_1 | 46 | 52 | PF00149 | 0.385 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.671 |
DOC_USP7_UBL2_3 | 135 | 139 | PF12436 | 0.781 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.803 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 134 | 142 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.561 |
LIG_APCC_ABBA_1 | 197 | 202 | PF00400 | 0.607 |
LIG_BIR_III_4 | 239 | 243 | PF00653 | 0.608 |
LIG_eIF4E_1 | 16 | 22 | PF01652 | 0.631 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.540 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.614 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.349 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.500 |
LIG_LIR_Gen_1 | 189 | 198 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.650 |
LIG_LYPXL_S_1 | 199 | 203 | PF13949 | 0.543 |
LIG_LYPXL_yS_3 | 200 | 203 | PF13949 | 0.547 |
LIG_NRBOX | 193 | 199 | PF00104 | 0.382 |
LIG_PCNA_yPIPBox_3 | 60 | 74 | PF02747 | 0.643 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.454 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.676 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.662 |
LIG_SUMO_SIM_anti_2 | 69 | 75 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 170 | 178 | PF11976 | 0.585 |
LIG_SUMO_SIM_par_1 | 293 | 300 | PF11976 | 0.585 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.627 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.635 |
LIG_TRAF2_1 | 84 | 87 | PF00917 | 0.444 |
LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.541 |
MOD_CDK_SPxxK_3 | 98 | 105 | PF00069 | 0.795 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.656 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.732 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.384 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.795 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.610 |
MOD_Cter_Amidation | 103 | 106 | PF01082 | 0.546 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.768 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.786 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.795 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.431 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.428 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.498 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.643 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.582 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.419 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.705 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.408 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.578 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.728 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.661 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.718 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.473 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.492 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.455 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.542 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.516 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.797 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.517 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.590 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.728 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.665 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.647 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.714 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.704 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.711 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.633 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.801 |
TRG_DiLeu_BaEn_1 | 259 | 264 | PF01217 | 0.676 |
TRG_DiLeu_BaEn_1 | 69 | 74 | PF01217 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 170 | 175 | PF01217 | 0.611 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.641 |
TRG_NES_CRM1_1 | 280 | 293 | PF08389 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYT7 | Leptomonas seymouri | 39% | 94% |
A0A3Q8IEH7 | Leishmania donovani | 71% | 100% |
A4I094 | Leishmania infantum | 71% | 100% |
C9ZV52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 84% |
E9ACS4 | Leishmania major | 67% | 100% |
E9AW58 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |