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. | no | 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_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.362 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.397 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.269 |
DEG_MDM2_SWIB_1 | 204 | 211 | PF02201 | 0.352 |
DOC_CYCLIN_RxL_1 | 272 | 281 | PF00134 | 0.198 |
DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.346 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.347 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.320 |
LIG_AP2alpha_2 | 101 | 103 | PF02296 | 0.371 |
LIG_BIR_III_4 | 206 | 210 | PF00653 | 0.344 |
LIG_BIR_III_4 | 234 | 238 | PF00653 | 0.389 |
LIG_CAP-Gly_1 | 324 | 328 | PF01302 | 0.337 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.229 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.356 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.324 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.418 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.352 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.391 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.368 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.352 |
LIG_LIR_Gen_1 | 177 | 185 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 33 | 42 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.369 |
LIG_LIR_LC3C_4 | 152 | 157 | PF02991 | 0.198 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 259 | 263 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.369 |
LIG_PDZ_Class_2 | 323 | 328 | PF00595 | 0.431 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.352 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.411 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 88 | 92 | PF00017 | 0.402 |
LIG_SH2_SRC | 250 | 253 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.366 |
LIG_SH3_2 | 270 | 275 | PF14604 | 0.314 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.280 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.352 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.335 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.484 |
LIG_SUMO_SIM_par_1 | 154 | 160 | PF11976 | 0.301 |
LIG_WRC_WIRS_1 | 245 | 250 | PF05994 | 0.352 |
LIG_WRC_WIRS_1 | 36 | 41 | PF05994 | 0.366 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.500 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.507 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.352 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.423 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.281 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.333 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.469 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.352 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.352 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.224 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.359 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.335 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.502 |
MOD_N-GLC_2 | 173 | 175 | PF02516 | 0.207 |
MOD_N-GLC_2 | 255 | 257 | PF02516 | 0.348 |
MOD_N-GLC_2 | 49 | 51 | PF02516 | 0.314 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.385 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.418 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.419 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.357 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.713 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.413 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.307 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.436 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.301 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.433 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.358 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.359 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.369 |
MOD_Plk_2-3 | 86 | 92 | PF00069 | 0.352 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.490 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.403 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.347 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.390 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.365 |
MOD_SUMO_rev_2 | 253 | 263 | PF00179 | 0.313 |
TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.220 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.398 |
TRG_NES_CRM1_1 | 148 | 160 | PF08389 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5W3 | Leptomonas seymouri | 57% | 100% |
A0A0N1HYU8 | Leptomonas seymouri | 55% | 100% |
A0A0N1I429 | Leptomonas seymouri | 79% | 100% |
A0A0N1I5D6 | Leptomonas seymouri | 51% | 100% |
A0A0N1I720 | Leptomonas seymouri | 60% | 100% |
A0A0N1IL04 | Leptomonas seymouri | 50% | 100% |
A0A0N1PCE9 | Leptomonas seymouri | 55% | 100% |
A0A0R6XPC0 | Leishmania donovani | 56% | 100% |
A0A3Q8IHB3 | Leishmania donovani | 53% | 100% |
A0A3S5H6H4 | Leishmania donovani | 95% | 100% |
A0A3S5H6H5 | Leishmania donovani | 57% | 100% |
A0A3S7WRC9 | Leishmania donovani | 55% | 100% |
A0A3S7WRD5 | Leishmania donovani | 53% | 100% |
A0A3S7WRE8 | Leishmania donovani | 50% | 100% |
A4H6B5 | Leishmania braziliensis | 81% | 100% |
A4H6B6 | Leishmania braziliensis | 51% | 100% |
A4H6B7 | Leishmania braziliensis | 57% | 100% |
A4H6B8 | Leishmania braziliensis | 50% | 100% |
A4H6B9 | Leishmania braziliensis | 58% | 100% |
A4H6C0 | Leishmania braziliensis | 53% | 100% |
A4H6C1 | Leishmania braziliensis | 51% | 100% |
A4HUN8 | Leishmania infantum | 95% | 100% |
A4HUN9 | Leishmania infantum | 53% | 100% |
A4HUP0 | Leishmania infantum | 56% | 100% |
A4HUP1 | Leishmania infantum | 53% | 100% |
A4HUP2 | Leishmania infantum | 57% | 100% |
A4HUP3 | Leishmania infantum | 54% | 100% |
A4HUP4 | Leishmania infantum | 50% | 100% |
E9AND7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AND8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AND9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9ANE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9ANE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9ANE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9ANE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
Q4QH83 | Leishmania major | 52% | 100% |
Q4QH84 | Leishmania major | 54% | 98% |
Q4QH85 | Leishmania major | 57% | 100% |
Q4QH86 | Leishmania major | 52% | 100% |
Q4QH87 | Leishmania major | 54% | 100% |
Q4QH88 | Leishmania major | 53% | 100% |