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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H619
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.654 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.512 |
CLV_PCSK_FUR_1 | 67 | 71 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.764 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.507 |
DEG_SPOP_SBC_1 | 212 | 216 | PF00917 | 0.550 |
DEG_SPOP_SBC_1 | 7 | 11 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.709 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.728 |
LIG_14-3-3_CanoR_1 | 218 | 226 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 69 | 77 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.610 |
LIG_Actin_WH2_2 | 53 | 71 | PF00022 | 0.586 |
LIG_CaM_NSCaTE_8 | 233 | 240 | PF13499 | 0.570 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.669 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.779 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.560 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.656 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.573 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.661 |
LIG_GBD_Chelix_1 | 127 | 135 | PF00786 | 0.606 |
LIG_LIR_Apic_2 | 145 | 149 | PF02991 | 0.559 |
LIG_PTB_Apo_2 | 136 | 143 | PF02174 | 0.450 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.528 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.500 |
LIG_SUMO_SIM_par_1 | 53 | 58 | PF11976 | 0.609 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.640 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.657 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.555 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.602 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.431 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.619 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.664 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.649 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.663 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.726 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.639 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.685 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.614 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.617 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.567 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.729 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.584 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.623 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.470 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.610 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.677 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.559 |
MOD_LATS_1 | 211 | 217 | PF00433 | 0.552 |
MOD_LATS_1 | 253 | 259 | PF00433 | 0.595 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.518 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.752 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.689 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.553 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.627 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.676 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.676 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.536 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.777 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.724 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.695 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.461 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.762 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.516 |
MOD_Plk_2-3 | 244 | 250 | PF00069 | 0.563 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.556 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.502 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.734 |
MOD_SUMO_rev_2 | 198 | 204 | PF00179 | 0.624 |
MOD_SUMO_rev_2 | 258 | 266 | PF00179 | 0.645 |
MOD_SUMO_rev_2 | 287 | 293 | PF00179 | 0.531 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.692 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.516 |
TRG_NLS_Bipartite_1 | 171 | 186 | PF00514 | 0.748 |
TRG_NLS_MonoExtN_4 | 179 | 186 | PF00514 | 0.751 |
TRG_Pf-PMV_PEXEL_1 | 172 | 176 | PF00026 | 0.716 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3L7 | Leptomonas seymouri | 54% | 100% |
A0A1X0NPM5 | Trypanosomatidae | 31% | 91% |
A0A3R7LS50 | Trypanosoma rangeli | 33% | 99% |
A4H559 | Leishmania braziliensis | 75% | 100% |
A4HTD6 | Leishmania infantum | 99% | 100% |
C9ZUH8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9ALC9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QIH6 | Leishmania major | 91% | 100% |
V5BYD2 | Trypanosoma cruzi | 34% | 90% |