Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 42 |
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: 24 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 42 |
NetGPI | no | yes: 0, no: 42 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.537 |
DEG_COP1_1 | 71 | 79 | PF00400 | 0.529 |
DOC_CDC14_PxL_1 | 73 | 81 | PF14671 | 0.348 |
DOC_MAPK_gen_1 | 14 | 22 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 152 | 161 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 15 | 24 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.458 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.329 |
DOC_PP4_FxxP_1 | 185 | 188 | PF00568 | 0.329 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.423 |
LIG_APCC_ABBA_1 | 62 | 67 | PF00400 | 0.448 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.464 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.455 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.453 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.446 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.480 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.476 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.487 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.301 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.464 |
LIG_LIR_Apic_2 | 184 | 188 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 71 | 79 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.481 |
LIG_MYND_3 | 259 | 263 | PF01753 | 0.320 |
LIG_PTB_Apo_2 | 225 | 232 | PF02174 | 0.466 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.464 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.622 |
LIG_SH2_GRB2like | 226 | 229 | PF00017 | 0.464 |
LIG_SH2_PTP2 | 226 | 229 | PF00017 | 0.329 |
LIG_SH2_SRC | 226 | 229 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.440 |
LIG_SH3_2 | 253 | 258 | PF14604 | 0.425 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.447 |
LIG_SUMO_SIM_par_1 | 138 | 144 | PF11976 | 0.411 |
LIG_TYR_ITSM | 222 | 229 | PF00017 | 0.492 |
LIG_WRC_WIRS_1 | 21 | 26 | PF05994 | 0.477 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.444 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.484 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.455 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.396 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.464 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.283 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.470 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.446 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.447 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.473 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.513 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.475 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.468 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.497 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.469 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.461 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.426 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.473 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.462 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.437 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.480 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.487 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.501 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.472 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.423 |
MOD_SUMO_for_1 | 91 | 94 | PF00179 | 0.437 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.491 |
TRG_NES_CRM1_1 | 132 | 144 | PF08389 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 238 | 243 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5W3 | Leptomonas seymouri | 60% | 98% |
A0A0N1HYU8 | Leptomonas seymouri | 58% | 98% |
A0A0N1I429 | Leptomonas seymouri | 51% | 95% |
A0A0N1I5D6 | Leptomonas seymouri | 65% | 99% |
A0A0N1I720 | Leptomonas seymouri | 54% | 99% |
A0A0N1IL04 | Leptomonas seymouri | 79% | 100% |
A0A0N1PCE9 | Leptomonas seymouri | 53% | 97% |
A0A0R6XPC0 | Leishmania donovani | 54% | 100% |
A0A3Q8IHB3 | Leishmania donovani | 51% | 100% |
A0A3S5H6H4 | Leishmania donovani | 50% | 100% |
A0A3S5H6H5 | Leishmania donovani | 55% | 99% |
A0A3S7WRC9 | Leishmania donovani | 65% | 100% |
A0A3S7WRD5 | Leishmania donovani | 69% | 100% |
A4H6B5 | Leishmania braziliensis | 52% | 100% |
A4H6B6 | Leishmania braziliensis | 50% | 100% |
A4H6B7 | Leishmania braziliensis | 55% | 100% |
A4H6B8 | Leishmania braziliensis | 70% | 100% |
A4H6B9 | Leishmania braziliensis | 57% | 100% |
A4H6C0 | Leishmania braziliensis | 63% | 100% |
A4H6C1 | Leishmania braziliensis | 85% | 100% |
A4HUN8 | Leishmania infantum | 50% | 100% |
A4HUN9 | Leishmania infantum | 51% | 100% |
A4HUP0 | Leishmania infantum | 55% | 100% |
A4HUP1 | Leishmania infantum | 69% | 100% |
A4HUP2 | Leishmania infantum | 55% | 99% |
A4HUP3 | Leishmania infantum | 65% | 100% |
A4HUP4 | Leishmania infantum | 100% | 100% |
E9AND7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AND8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AND9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9ANE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
E9ANE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 99% |
E9ANE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
E9ANE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QH83 | Leishmania major | 94% | 100% |
Q4QH84 | Leishmania major | 66% | 100% |
Q4QH85 | Leishmania major | 56% | 99% |
Q4QH86 | Leishmania major | 72% | 100% |
Q4QH87 | Leishmania major | 56% | 100% |
Q4QH88 | Leishmania major | 51% | 100% |
Q4QH89 | Leishmania major | 50% | 100% |