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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AT93
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 7 |
GO:0008047 | enzyme activator activity | 3 | 7 |
GO:0030234 | enzyme regulator activity | 2 | 7 |
GO:0030695 | GTPase regulator activity | 4 | 7 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 7 |
GO:0098772 | molecular function regulator activity | 1 | 7 |
GO:0140677 | molecular function activator activity | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.319 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.411 |
CLV_Separin_Metazoa | 13 | 17 | PF03568 | 0.436 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.474 |
DEG_COP1_1 | 153 | 162 | PF00400 | 0.519 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.700 |
DEG_SPOP_SBC_1 | 193 | 197 | PF00917 | 0.637 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.626 |
DOC_MAPK_MEF2A_6 | 107 | 114 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 109 | 115 | PF00149 | 0.338 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.689 |
DOC_PP4_FxxP_1 | 329 | 332 | PF00568 | 0.585 |
DOC_SPAK_OSR1_1 | 76 | 80 | PF12202 | 0.513 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.592 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.803 |
LIG_14-3-3_CanoR_1 | 287 | 297 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 4 | 14 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 76 | 80 | PF00244 | 0.436 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.794 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.411 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.375 |
LIG_IBAR_NPY_1 | 338 | 340 | PF08397 | 0.594 |
LIG_LIR_Apic_2 | 186 | 192 | PF02991 | 0.690 |
LIG_LIR_Apic_2 | 326 | 332 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 124 | 130 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 153 | 163 | PF02991 | 0.763 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 124 | 128 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.765 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.715 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.416 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.411 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.810 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.798 |
LIG_SH2_STAT3 | 296 | 299 | PF00017 | 0.703 |
LIG_SH2_STAT3 | 340 | 343 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.411 |
LIG_SH3_2 | 173 | 178 | PF14604 | 0.751 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.741 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.671 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.682 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.684 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.633 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.656 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.561 |
LIG_SUMO_SIM_par_1 | 143 | 149 | PF11976 | 0.639 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.280 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.738 |
LIG_WRC_WIRS_1 | 90 | 95 | PF05994 | 0.513 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.559 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.733 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.692 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.593 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.443 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.513 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.734 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.411 |
MOD_GlcNHglycan | 124 | 128 | PF01048 | 0.515 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.722 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.754 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.743 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.714 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.504 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.588 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.753 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.328 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.397 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.299 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.627 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.747 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.795 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.700 |
MOD_N-GLC_1 | 273 | 278 | PF02516 | 0.718 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.805 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.706 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.809 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.411 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.494 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.675 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.411 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.795 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.541 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.583 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.411 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.615 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.436 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.621 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.633 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.794 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.533 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.799 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.589 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.681 |
TRG_Pf-PMV_PEXEL_1 | 16 | 20 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XB38 | Leishmania donovani | 87% | 75% |
A4HPI1 | Leishmania braziliensis | 66% | 100% |
A4IDA3 | Leishmania infantum | 87% | 75% |
D0A8E3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 99% |
Q4Q1A4 | Leishmania major | 80% | 100% |