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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9APK0
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0003924 | GTPase activity | 7 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005525 | GTP binding | 5 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0019001 | guanyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.721 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.597 |
DOC_MAPK_gen_1 | 57 | 64 | PF00069 | 0.689 |
DOC_MAPK_MEF2A_6 | 57 | 64 | PF00069 | 0.655 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.563 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 116 | 125 | PF00244 | 0.648 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.594 |
LIG_eIF4E_1 | 25 | 31 | PF01652 | 0.645 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.542 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.578 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.600 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.699 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.559 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.677 |
LIG_LIR_Gen_1 | 74 | 79 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 91 | 100 | PF02991 | 0.694 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.613 |
LIG_SH2_STAT3 | 117 | 120 | PF00017 | 0.699 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.653 |
LIG_SUMO_SIM_par_1 | 164 | 170 | PF11976 | 0.664 |
LIG_SUMO_SIM_par_1 | 60 | 66 | PF11976 | 0.632 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.601 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.685 |
LIG_WRC_WIRS_1 | 149 | 154 | PF05994 | 0.634 |
MOD_CDK_SPxxK_3 | 50 | 57 | PF00069 | 0.698 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.757 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.692 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.558 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.768 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.634 |
MOD_GlcNHglycan | 86 | 91 | PF01048 | 0.690 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.563 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.640 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.645 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.628 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.647 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.553 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.713 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.658 |
MOD_PK_1 | 137 | 143 | PF00069 | 0.679 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.712 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.575 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.637 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.620 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.587 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.710 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.675 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBE8 | Leptomonas seymouri | 61% | 78% |
A0A1X0NNU1 | Trypanosomatidae | 36% | 100% |
A0A3R7LA27 | Trypanosoma rangeli | 42% | 100% |
A0A3S7WSS1 | Leishmania donovani | 96% | 100% |
A4H7G7 | Leishmania braziliensis | 87% | 100% |
A4HVU8 | Leishmania infantum | 97% | 100% |
C9ZT78 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4QFX9 | Leishmania major | 93% | 100% |
V5DE15 | Trypanosoma cruzi | 41% | 100% |