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: 7 |
NetGPI | no | yes: 0, no: 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.599 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.521 |
CLV_PCSK_FUR_1 | 38 | 42 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.575 |
CLV_Separin_Metazoa | 264 | 268 | PF03568 | 0.508 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.675 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.725 |
DOC_CDC14_PxL_1 | 300 | 308 | PF14671 | 0.474 |
DOC_CYCLIN_RxL_1 | 195 | 205 | PF00134 | 0.574 |
DOC_MAPK_gen_1 | 187 | 198 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 38 | 47 | PF00069 | 0.687 |
DOC_MAPK_MEF2A_6 | 201 | 208 | PF00069 | 0.427 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.517 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 239 | 249 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.546 |
LIG_BIR_III_4 | 29 | 33 | PF00653 | 0.543 |
LIG_CtBP_PxDLS_1 | 76 | 80 | PF00389 | 0.624 |
LIG_eIF4E_1 | 105 | 111 | PF01652 | 0.447 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.567 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.484 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.471 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.421 |
LIG_LIR_Apic_2 | 70 | 76 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 310 | 321 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.533 |
LIG_PCNA_TLS_4 | 201 | 208 | PF02747 | 0.461 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.531 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.504 |
LIG_SH2_SRC | 207 | 210 | PF00017 | 0.611 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.427 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.470 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.591 |
LIG_TRFH_1 | 105 | 109 | PF08558 | 0.440 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.431 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.506 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.721 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.496 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.468 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.519 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.601 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.568 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.756 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.678 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.606 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.629 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.689 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.351 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.630 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.497 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.495 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.467 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.688 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.557 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.580 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.526 |
MOD_PKA_1 | 188 | 194 | PF00069 | 0.562 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.595 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.718 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.539 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.548 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.397 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.407 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.440 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.554 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.528 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.513 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.539 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.589 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 38 | 41 | PF00400 | 0.740 |
TRG_Pf-PMV_PEXEL_1 | 100 | 104 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF7 | Leptomonas seymouri | 59% | 100% |
A0A1X0NWV8 | Trypanosomatidae | 34% | 100% |
A0A3S7WYC1 | Leishmania donovani | 90% | 100% |
A4I0S5 | Leishmania infantum | 90% | 100% |
D0A755 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AIG8 | Leishmania braziliensis | 76% | 100% |
Q4QAP7 | Leishmania major | 89% | 100% |