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 |
Related structures:
AlphaFold database: A0A3Q8ICV5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.562 |
DEG_COP1_1 | 238 | 246 | PF00400 | 0.376 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.627 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.425 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 310 | 317 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 317 | 323 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 235 | 243 | PF00069 | 0.434 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.550 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.365 |
LIG_14-3-3_CanoR_1 | 142 | 147 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.632 |
LIG_Actin_WH2_2 | 59 | 75 | PF00022 | 0.369 |
LIG_APCC_ABBA_1 | 16 | 21 | PF00400 | 0.571 |
LIG_BIR_III_2 | 251 | 255 | PF00653 | 0.330 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.438 |
LIG_DLG_GKlike_1 | 142 | 150 | PF00625 | 0.357 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.334 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.518 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.439 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.490 |
LIG_LIR_Apic_2 | 101 | 106 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.351 |
LIG_MYND_1 | 244 | 248 | PF01753 | 0.313 |
LIG_MYND_3 | 253 | 257 | PF01753 | 0.379 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.448 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.446 |
LIG_REV1ctd_RIR_1 | 203 | 211 | PF16727 | 0.441 |
LIG_REV1ctd_RIR_1 | 231 | 241 | PF16727 | 0.409 |
LIG_REV1ctd_RIR_1 | 285 | 294 | PF16727 | 0.486 |
LIG_REV1ctd_RIR_1 | 326 | 335 | PF16727 | 0.354 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.482 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.481 |
LIG_SH2_NCK_1 | 103 | 107 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.391 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.449 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.381 |
LIG_SUMO_SIM_par_1 | 335 | 341 | PF11976 | 0.411 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.377 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.312 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.474 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.366 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.488 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.468 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.382 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.466 |
MOD_GlcNHglycan | 177 | 182 | PF01048 | 0.494 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.441 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.348 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.426 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.417 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.618 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.326 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.391 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.371 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.621 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.428 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.357 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.379 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.457 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.569 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.394 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.461 |
MOD_PKA_1 | 38 | 44 | PF00069 | 0.425 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.635 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.438 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.459 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.358 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.453 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.342 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.343 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.419 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.314 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.371 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.545 |
TRG_DiLeu_BaEn_2 | 120 | 126 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_4 | 178 | 184 | PF01217 | 0.578 |
TRG_DiLeu_LyEn_5 | 366 | 371 | PF01217 | 0.635 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.477 |
TRG_NLS_MonoCore_2 | 23 | 28 | PF00514 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 369 | 374 | PF00026 | 0.594 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2W1 | Leptomonas seymouri | 74% | 100% |
A0A0S4ISK5 | Bodo saltans | 46% | 100% |
A0A1X0NRI0 | Trypanosomatidae | 54% | 100% |
A4HFZ3 | Leishmania braziliensis | 89% | 100% |
A4I312 | Leishmania infantum | 100% | 100% |
C9ZJH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9ADJ6 | Leishmania major | 97% | 100% |
E9AZC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5BNB6 | Trypanosoma cruzi | 60% | 100% |