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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.816 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.488 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.669 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.598 |
DOC_CKS1_1 | 228 | 233 | PF01111 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 204 | 210 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 174 | 182 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 165 | 173 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 80 | 87 | PF00069 | 0.587 |
DOC_MAPK_NFAT4_5 | 80 | 88 | PF00069 | 0.589 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.684 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.577 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 145 | 153 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 174 | 182 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 302 | 308 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 357 | 363 | PF00244 | 0.599 |
LIG_CtBP_PxDLS_1 | 73 | 77 | PF00389 | 0.436 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.577 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.512 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.649 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.343 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.497 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.556 |
LIG_LIR_Apic_2 | 205 | 209 | PF02991 | 0.480 |
LIG_LIR_Apic_2 | 225 | 231 | PF02991 | 0.758 |
LIG_LIR_Apic_2 | 257 | 262 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 214 | 222 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.402 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.665 |
LIG_SH2_CRK | 228 | 232 | PF00017 | 0.732 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.368 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.637 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 228 | 232 | PF00017 | 0.732 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 55 | 58 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.557 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.659 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.660 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.524 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.622 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.550 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.508 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.788 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.748 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.552 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.551 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.575 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.777 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.772 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.621 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.574 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.550 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.443 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.537 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.496 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.624 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.655 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.675 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.596 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.422 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.457 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.652 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.485 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.645 |
MOD_PKA_1 | 356 | 362 | PF00069 | 0.643 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.459 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.510 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.533 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.564 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.643 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.772 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.671 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.575 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.710 |
MOD_Plk_2-3 | 110 | 116 | PF00069 | 0.759 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.566 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.439 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.681 |
MOD_SUMO_rev_2 | 346 | 353 | PF00179 | 0.628 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.638 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.515 |
TRG_NLS_MonoExtC_3 | 355 | 360 | PF00514 | 0.654 |
TRG_NLS_MonoExtN_4 | 356 | 361 | PF00514 | 0.644 |
TRG_Pf-PMV_PEXEL_1 | 313 | 318 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM80 | Leptomonas seymouri | 68% | 100% |
A0A3Q8IDC8 | Leishmania donovani | 84% | 100% |
A4HYE1 | Leishmania infantum | 84% | 100% |
E9AS74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QD92 | Leishmania major | 82% | 99% |