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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HDR1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.562 |
CLV_PCSK_FUR_1 | 107 | 111 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.454 |
DEG_SCF_FBW7_2 | 319 | 326 | PF00400 | 0.452 |
DOC_MAPK_gen_1 | 96 | 104 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 297 | 304 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 97 | 106 | PF00069 | 0.572 |
DOC_PP1_RVXF_1 | 5 | 11 | PF00149 | 0.608 |
DOC_PP1_SILK_1 | 32 | 37 | PF00149 | 0.377 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.537 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.494 |
LIG_14-3-3_CanoR_1 | 108 | 117 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 208 | 215 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 249 | 255 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.519 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.536 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.379 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.582 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.526 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.557 |
LIG_Pex14_1 | 175 | 179 | PF04695 | 0.689 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.532 |
LIG_SH2_GRB2like | 16 | 19 | PF00017 | 0.564 |
LIG_SH2_NCK_1 | 57 | 61 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.463 |
LIG_SH3_1 | 160 | 166 | PF00018 | 0.506 |
LIG_SH3_2 | 316 | 321 | PF14604 | 0.609 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.559 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.648 |
LIG_SUMO_SIM_par_1 | 100 | 105 | PF11976 | 0.374 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.469 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.598 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.517 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.375 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.506 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.505 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.589 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.629 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.585 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.753 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.581 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.538 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.543 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.474 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.412 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.685 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.659 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.660 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.564 |
MOD_PK_1 | 30 | 36 | PF00069 | 0.557 |
MOD_PKA_1 | 109 | 115 | PF00069 | 0.378 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.473 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.776 |
MOD_PKB_1 | 107 | 115 | PF00069 | 0.572 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.361 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.393 |
MOD_Plk_2-3 | 326 | 332 | PF00069 | 0.587 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.507 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.435 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.660 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.441 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.490 |
MOD_SUMO_for_1 | 81 | 84 | PF00179 | 0.482 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3P5 | Leptomonas seymouri | 49% | 100% |
A0A3Q8ID13 | Leishmania donovani | 73% | 100% |
A0A422NWQ4 | Trypanosoma rangeli | 33% | 100% |
A4I107 | Leishmania infantum | 74% | 99% |
C9ZWA2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AX45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 99% |
Q4QAD1 | Leishmania major | 76% | 100% |
V5BJJ9 | Trypanosoma cruzi | 32% | 100% |