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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HM21
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004252 | serine-type endopeptidase activity | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008236 | serine-type peptidase activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0017171 | serine hydrolase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.739 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.495 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.706 |
DOC_CYCLIN_RxL_1 | 36 | 47 | PF00134 | 0.636 |
DOC_MAPK_DCC_7 | 20 | 30 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 20 | 27 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 223 | 233 | PF00069 | 0.739 |
DOC_MAPK_JIP1_4 | 39 | 45 | PF00069 | 0.636 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.644 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 63 | 72 | PF00069 | 0.553 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.560 |
DOC_PP2B_LxvP_1 | 91 | 94 | PF13499 | 0.587 |
DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.601 |
DOC_SPAK_OSR1_1 | 101 | 105 | PF12202 | 0.627 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.650 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 115 | 124 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.740 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.770 |
LIG_BIR_III_4 | 235 | 239 | PF00653 | 0.738 |
LIG_Clathr_ClatBox_1 | 137 | 141 | PF01394 | 0.698 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.546 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.613 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.677 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.591 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.730 |
LIG_LIR_Apic_2 | 144 | 148 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 29 | 38 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 29 | 33 | PF02991 | 0.584 |
LIG_Rb_LxCxE_1 | 165 | 179 | PF01857 | 0.457 |
LIG_SH2_STAP1 | 84 | 88 | PF00017 | 0.736 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.656 |
LIG_SUMO_SIM_anti_2 | 134 | 139 | PF11976 | 0.595 |
LIG_SUMO_SIM_anti_2 | 230 | 235 | PF11976 | 0.717 |
LIG_SUMO_SIM_anti_2 | 69 | 74 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.664 |
LIG_SUMO_SIM_par_1 | 228 | 235 | PF11976 | 0.742 |
LIG_SUMO_SIM_par_1 | 69 | 74 | PF11976 | 0.467 |
LIG_UBA3_1 | 27 | 36 | PF00899 | 0.690 |
LIG_WRC_WIRS_1 | 27 | 32 | PF05994 | 0.612 |
LIG_WW_1 | 94 | 97 | PF00397 | 0.444 |
MOD_CDK_SPK_2 | 50 | 55 | PF00069 | 0.468 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.633 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.549 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.658 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.679 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.641 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.573 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.539 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.598 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.475 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.579 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.583 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.720 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.711 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.506 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.717 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.487 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.711 |
MOD_Plk_2-3 | 193 | 199 | PF00069 | 0.643 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.699 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.670 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.682 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.574 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.686 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.706 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.607 |
MOD_SUMO_rev_2 | 216 | 225 | PF00179 | 0.610 |
TRG_DiLeu_BaEn_1 | 209 | 214 | PF01217 | 0.661 |
TRG_DiLeu_BaLyEn_6 | 122 | 127 | PF01217 | 0.715 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.570 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6J2 | Leptomonas seymouri | 56% | 85% |
A0A0S4J2F7 | Bodo saltans | 40% | 84% |
A0A0S4JI53 | Bodo saltans | 40% | 86% |
A0A1X0NRD6 | Trypanosomatidae | 43% | 83% |
A0A3Q8IHS3 | Leishmania donovani | 80% | 83% |
A4I9F4 | Leishmania infantum | 80% | 83% |
C9ZJS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 83% |
E9B4F2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 83% |
Q4Q3M3 | Leishmania major | 81% | 100% |
V5D3Q6 | Trypanosoma cruzi | 46% | 90% |