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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HWI4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 292 | 296 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.514 |
CLV_Separin_Metazoa | 51 | 55 | PF03568 | 0.400 |
DEG_SPOP_SBC_1 | 221 | 225 | PF00917 | 0.690 |
DEG_SPOP_SBC_1 | 60 | 64 | PF00917 | 0.580 |
DOC_ANK_TNKS_1 | 66 | 73 | PF00023 | 0.632 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.500 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.654 |
DOC_USP7_MATH_2 | 208 | 214 | PF00917 | 0.572 |
DOC_USP7_UBL2_3 | 198 | 202 | PF12436 | 0.590 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.625 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.621 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.494 |
LIG_14-3-3_CanoR_1 | 112 | 119 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 186 | 204 | PF00022 | 0.477 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.650 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.625 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.625 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.551 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.580 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.498 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.393 |
LIG_LIR_Gen_1 | 213 | 222 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 299 | 310 | PF02991 | 0.671 |
LIG_LIR_Gen_1 | 93 | 102 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.389 |
LIG_NRP_CendR_1 | 320 | 323 | PF00754 | 0.632 |
LIG_PTAP_UEV_1 | 3 | 8 | PF05743 | 0.592 |
LIG_SH2_PTP2 | 27 | 30 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.489 |
LIG_SH3_1 | 241 | 247 | PF00018 | 0.521 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.749 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.699 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.687 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.659 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 144 | 159 | PF11976 | 0.554 |
LIG_SUMO_SIM_anti_2 | 314 | 320 | PF11976 | 0.530 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.625 |
LIG_TRAF2_1 | 22 | 25 | PF00917 | 0.514 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.714 |
LIG_WW_2 | 278 | 281 | PF00397 | 0.647 |
LIG_WW_3 | 245 | 249 | PF00397 | 0.659 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.646 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.710 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.687 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.693 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.629 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.625 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.690 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.687 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.776 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.561 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.580 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.709 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.628 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.591 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.662 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.711 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.640 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.723 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.570 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.522 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.764 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.632 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.768 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.634 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.702 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.636 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.659 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.716 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.546 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.543 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.498 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.719 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.609 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.673 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.715 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.649 |
MOD_Plk_2-3 | 153 | 159 | PF00069 | 0.613 |
MOD_Plk_2-3 | 161 | 167 | PF00069 | 0.541 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.673 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.670 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.752 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.724 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.604 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.642 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WTH2 | Leishmania donovani | 99% | 100% |
A4H858 | Leishmania braziliensis | 57% | 96% |
E9AQ85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 96% |
Q4QF98 | Leishmania major | 87% | 100% |