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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q8Z8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.526 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.520 |
DEG_SPOP_SBC_1 | 166 | 170 | PF00917 | 0.434 |
DEG_SPOP_SBC_1 | 183 | 187 | PF00917 | 0.502 |
DOC_CKS1_1 | 284 | 289 | PF01111 | 0.657 |
DOC_CKS1_1 | 56 | 61 | PF01111 | 0.652 |
DOC_CYCLIN_yCln2_LP_2 | 164 | 167 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 216 | 222 | PF00134 | 0.549 |
DOC_MAPK_gen_1 | 118 | 127 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 149 | 159 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 204 | 212 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 8 | 17 | PF00069 | 0.548 |
DOC_PP1_RVXF_1 | 118 | 125 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 133 | 139 | PF00149 | 0.270 |
DOC_PP2B_LxvP_1 | 164 | 167 | PF13499 | 0.491 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.577 |
DOC_PP4_FxxP_1 | 172 | 175 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.522 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.627 |
DOC_USP7_UBL2_3 | 201 | 205 | PF12436 | 0.491 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 120 | 125 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 156 | 166 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 251 | 257 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 320 | 329 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 330 | 335 | PF00244 | 0.691 |
LIG_APCC_ABBAyCdc20_2 | 189 | 195 | PF00400 | 0.491 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.599 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.549 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.491 |
LIG_eIF4E_1 | 93 | 99 | PF01652 | 0.545 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.370 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.548 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.725 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.662 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.491 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.637 |
LIG_HCF-1_HBM_1 | 282 | 285 | PF13415 | 0.483 |
LIG_LIR_Apic_2 | 169 | 175 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 77 | 88 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 123 | 127 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.444 |
LIG_Pex14_2 | 66 | 70 | PF04695 | 0.522 |
LIG_PTB_Apo_2 | 104 | 111 | PF02174 | 0.370 |
LIG_PTB_Phospho_1 | 104 | 110 | PF10480 | 0.370 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.452 |
LIG_SH2_SRC | 193 | 196 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.406 |
LIG_SH3_1 | 72 | 78 | PF00018 | 0.545 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.421 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.660 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.728 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.637 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.505 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.391 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.680 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.633 |
MOD_CDK_SPK_2 | 55 | 60 | PF00069 | 0.650 |
MOD_CDK_SPxxK_3 | 55 | 62 | PF00069 | 0.430 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.423 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.365 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.754 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.625 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.467 |
MOD_CMANNOS | 65 | 68 | PF00535 | 0.482 |
MOD_Cter_Amidation | 202 | 205 | PF01082 | 0.491 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.583 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.609 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.640 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.732 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.366 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.561 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.766 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.420 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.377 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.576 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.700 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.500 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.557 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.648 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.680 |
MOD_PKB_1 | 118 | 126 | PF00069 | 0.491 |
MOD_PKB_1 | 249 | 257 | PF00069 | 0.651 |
MOD_PKB_1 | 328 | 336 | PF00069 | 0.555 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.423 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.532 |
MOD_Plk_2-3 | 267 | 273 | PF00069 | 0.538 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.482 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.471 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.695 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.527 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.441 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.653 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.777 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.651 |
MOD_SUMO_for_1 | 220 | 223 | PF00179 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 59 | 62 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.506 |
TRG_NES_CRM1_1 | 86 | 101 | PF08389 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 190 | 195 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 72 | 77 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.423 |
TRG_PTS1 | 353 | 356 | PF00515 | 0.627 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9E3 | Leptomonas seymouri | 45% | 100% |
A0A3Q8ICX4 | Leishmania donovani | 91% | 100% |
A4I2C2 | Leishmania infantum | 93% | 100% |
E9AYH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
V5D437 | Trypanosoma cruzi | 33% | 100% |