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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.490 |
CLV_PCSK_PC1ET2_1 | 60 | 62 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.406 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.709 |
DOC_MAPK_gen_1 | 162 | 170 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 261 | 269 | PF00069 | 0.561 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.465 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.540 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.478 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.439 |
LIG_APCC_ABBA_1 | 236 | 241 | PF00400 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 166 | 170 | PF00928 | 0.591 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.728 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.500 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.481 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.263 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.443 |
LIG_LIR_Gen_1 | 165 | 175 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 278 | 289 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 76 | 86 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.480 |
LIG_LYPXL_yS_3 | 158 | 161 | PF13949 | 0.499 |
LIG_MYND_1 | 131 | 135 | PF01753 | 0.494 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.557 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.588 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 78 | 82 | PF00017 | 0.560 |
LIG_SH2_PTP2 | 221 | 224 | PF00017 | 0.430 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.508 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.432 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.510 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.401 |
LIG_TYR_ITIM | 279 | 284 | PF00017 | 0.530 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.556 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.456 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.603 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.556 |
MOD_LATS_1 | 127 | 133 | PF00433 | 0.649 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.549 |
MOD_PKA_1 | 129 | 135 | PF00069 | 0.497 |
MOD_PKA_1 | 162 | 168 | PF00069 | 0.535 |
MOD_PKA_1 | 21 | 27 | PF00069 | 0.557 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.497 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.673 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.452 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.565 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.459 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.418 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.529 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.605 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.613 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.475 |
MOD_SUMO_for_1 | 191 | 194 | PF00179 | 0.583 |
MOD_SUMO_rev_2 | 79 | 86 | PF00179 | 0.556 |
TRG_DiLeu_BaEn_1 | 114 | 119 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_4 | 102 | 108 | PF01217 | 0.538 |
TRG_DiLeu_BaEn_4 | 114 | 120 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 89 | 94 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.556 |
TRG_NES_CRM1_1 | 99 | 111 | PF08389 | 0.486 |
TRG_NLS_MonoExtC_3 | 58 | 64 | PF00514 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 105 | 110 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4Q5 | Leptomonas seymouri | 81% | 100% |
A0A0S4JF52 | Bodo saltans | 52% | 100% |
A0A1X0P198 | Trypanosomatidae | 66% | 100% |
A0A3Q8IDR8 | Leishmania donovani | 98% | 100% |
A0A3R7MCA1 | Trypanosoma rangeli | 68% | 100% |
A4HLK0 | Leishmania braziliensis | 91% | 100% |
A4I911 | Leishmania infantum | 98% | 100% |
D0A511 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
Q4Q448 | Leishmania major | 98% | 100% |
V5BHC0 | Trypanosoma cruzi | 67% | 100% |