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: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AIX8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.452 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.568 |
DOC_ANK_TNKS_1 | 220 | 227 | PF00023 | 0.350 |
DOC_CYCLIN_RxL_1 | 55 | 64 | PF00134 | 0.519 |
DOC_PP1_RVXF_1 | 238 | 245 | PF00149 | 0.394 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.692 |
DOC_USP7_MATH_2 | 271 | 277 | PF00917 | 0.605 |
LIG_14-3-3_CanoR_1 | 129 | 135 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 186 | 194 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 6 | 23 | PF00022 | 0.583 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.635 |
LIG_BIR_III_4 | 203 | 207 | PF00653 | 0.334 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 170 | 174 | PF00533 | 0.259 |
LIG_deltaCOP1_diTrp_1 | 201 | 209 | PF00928 | 0.290 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.272 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.393 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.552 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.378 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.392 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.508 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.722 |
LIG_Pex14_2 | 210 | 214 | PF04695 | 0.441 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.189 |
LIG_SH2_STAT3 | 41 | 44 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.330 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.367 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.390 |
LIG_SUMO_SIM_anti_2 | 76 | 85 | PF11976 | 0.465 |
LIG_UBA3_1 | 81 | 85 | PF00899 | 0.480 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.275 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.353 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.597 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.554 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.336 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.478 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.734 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.393 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.564 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.536 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.574 |
MOD_GlcNHglycan | 124 | 128 | PF01048 | 0.432 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.365 |
MOD_GlcNHglycan | 178 | 182 | PF01048 | 0.555 |
MOD_GlcNHglycan | 31 | 35 | PF01048 | 0.622 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.426 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.632 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.731 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.344 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.317 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.449 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.536 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.605 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.558 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.683 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.463 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.469 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.505 |
MOD_N-GLC_2 | 155 | 157 | PF02516 | 0.502 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.412 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.283 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.524 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.457 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.462 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.638 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.302 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.532 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.502 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.555 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.351 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.561 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.470 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.358 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.332 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.495 |
MOD_Plk_2-3 | 110 | 116 | PF00069 | 0.381 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.381 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.330 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.266 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.247 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.372 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.367 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.506 |
TRG_DiLeu_BaEn_1 | 15 | 20 | PF01217 | 0.562 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 58 | 63 | PF00026 | 0.615 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIJ6 | Leptomonas seymouri | 57% | 100% |
A0A1X0NM60 | Trypanosomatidae | 39% | 100% |
A0A3Q8IKT7 | Leishmania donovani | 81% | 88% |
A0A422N6R3 | Trypanosoma rangeli | 42% | 100% |
A4ICH5 | Leishmania infantum | 81% | 88% |
E9AT46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 89% |
Q4Q1F2 | Leishmania major | 82% | 100% |
V5BPS4 | Trypanosoma cruzi | 43% | 100% |