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_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.373 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.410 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.387 |
DEG_COP1_1 | 75 | 84 | PF00400 | 0.452 |
DOC_MAPK_gen_1 | 18 | 26 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 19 | 28 | PF00069 | 0.474 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.385 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.418 |
LIG_14-3-3_CanoR_1 | 113 | 118 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 157 | 166 | PF00244 | 0.381 |
LIG_AP2alpha_2 | 90 | 92 | PF02296 | 0.405 |
LIG_APCC_ABBA_1 | 66 | 71 | PF00400 | 0.369 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.562 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.385 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.377 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.383 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.397 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.424 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.385 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 285 | 290 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 32 | 37 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.402 |
LIG_PDZ_Class_2 | 311 | 316 | PF00595 | 0.476 |
LIG_PTB_Apo_2 | 230 | 237 | PF02174 | 0.388 |
LIG_Rb_LxCxE_1 | 137 | 156 | PF01857 | 0.263 |
LIG_REV1ctd_RIR_1 | 119 | 127 | PF16727 | 0.342 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.385 |
LIG_SH2_CRK | 234 | 238 | PF00017 | 0.396 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.385 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.276 |
LIG_SH2_GRB2like | 231 | 234 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.385 |
LIG_SH3_2 | 258 | 263 | PF14604 | 0.347 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.348 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.385 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.369 |
LIG_TRFH_1 | 236 | 240 | PF08558 | 0.385 |
LIG_TYR_ITIM | 232 | 237 | PF00017 | 0.385 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.399 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.425 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.451 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.377 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.385 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.385 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.392 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.367 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.395 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.254 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.398 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.389 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.383 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.292 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.418 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.396 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.390 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.390 |
MOD_NEK2_2 | 252 | 257 | PF00069 | 0.348 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.442 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.385 |
MOD_PKB_1 | 106 | 114 | PF00069 | 0.385 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.384 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.359 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.402 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.408 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.423 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.394 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.367 |
MOD_SUMO_for_1 | 262 | 265 | PF00179 | 0.385 |
MOD_SUMO_for_1 | 96 | 99 | PF00179 | 0.359 |
MOD_SUMO_rev_2 | 235 | 245 | PF00179 | 0.364 |
MOD_SUMO_rev_2 | 3 | 13 | PF00179 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 110 | 115 | PF01217 | 0.263 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.270 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5W3 | Leptomonas seymouri | 80% | 100% |
A0A0N1HYU8 | Leptomonas seymouri | 64% | 99% |
A0A0N1I429 | Leptomonas seymouri | 54% | 97% |
A0A0N1I5D6 | Leptomonas seymouri | 59% | 100% |
A0A0N1I720 | Leptomonas seymouri | 55% | 100% |
A0A0N1IL04 | Leptomonas seymouri | 62% | 100% |
A0A0N1PCE9 | Leptomonas seymouri | 52% | 98% |
A0A0R6XPC0 | Leishmania donovani | 64% | 99% |
A0A3Q8IHB3 | Leishmania donovani | 48% | 98% |
A0A3S5H6H4 | Leishmania donovani | 53% | 96% |
A0A3S5H6H5 | Leishmania donovani | 58% | 100% |
A0A3S7WRC9 | Leishmania donovani | 97% | 100% |
A0A3S7WRD5 | Leishmania donovani | 63% | 100% |
A0A3S7WRE8 | Leishmania donovani | 66% | 100% |
A4H6B5 | Leishmania braziliensis | 53% | 96% |
A4H6B6 | Leishmania braziliensis | 48% | 99% |
A4H6B7 | Leishmania braziliensis | 65% | 99% |
A4H6B8 | Leishmania braziliensis | 63% | 100% |
A4H6B9 | Leishmania braziliensis | 57% | 100% |
A4H6C0 | Leishmania braziliensis | 89% | 100% |
A4H6C1 | Leishmania braziliensis | 64% | 100% |
A4HUN8 | Leishmania infantum | 53% | 96% |
A4HUN9 | Leishmania infantum | 48% | 98% |
A4HUP0 | Leishmania infantum | 65% | 99% |
A4HUP1 | Leishmania infantum | 63% | 100% |
A4HUP2 | Leishmania infantum | 58% | 100% |
A4HUP3 | Leishmania infantum | 97% | 100% |
A4HUP4 | Leishmania infantum | 66% | 100% |
E9AND7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 96% |
E9AND8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 98% |
E9AND9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 99% |
E9ANE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9ANE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
E9ANE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9ANE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
Q4QH83 | Leishmania major | 65% | 100% |
Q4QH85 | Leishmania major | 57% | 100% |
Q4QH86 | Leishmania major | 64% | 100% |
Q4QH87 | Leishmania major | 64% | 99% |
Q4QH88 | Leishmania major | 48% | 98% |
Q4QH89 | Leishmania major | 54% | 96% |