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: 10 |
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: E9ADN4
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 11 |
GO:0008047 | enzyme activator activity | 3 | 11 |
GO:0030234 | enzyme regulator activity | 2 | 11 |
GO:0030695 | GTPase regulator activity | 4 | 11 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 11 |
GO:0098772 | molecular function regulator activity | 1 | 11 |
GO:0140677 | molecular function activator activity | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.509 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 277 | 283 | PF00082 | 0.585 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.370 |
DEG_ODPH_VHL_1 | 292 | 303 | PF01847 | 0.422 |
DEG_SPOP_SBC_1 | 237 | 241 | PF00917 | 0.573 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.686 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.525 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 202 | 211 | PF00134 | 0.411 |
DOC_PP2B_LxvP_1 | 66 | 69 | PF13499 | 0.525 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.758 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.626 |
DOC_USP7_UBL2_3 | 47 | 51 | PF12436 | 0.649 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.208 |
LIG_14-3-3_CanoR_1 | 146 | 150 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 242 | 250 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 287 | 294 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 314 | 320 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 8 | 18 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 92 | 101 | PF00244 | 0.486 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_deltaCOP1_diTrp_1 | 312 | 322 | PF00928 | 0.503 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.503 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.545 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.683 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.310 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.307 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.830 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.609 |
LIG_Integrin_RGD_1 | 260 | 262 | PF01839 | 0.589 |
LIG_LIR_Apic_2 | 217 | 223 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.529 |
LIG_PCNA_PIPBox_1 | 208 | 217 | PF02747 | 0.318 |
LIG_PCNA_yPIPBox_3 | 205 | 215 | PF02747 | 0.311 |
LIG_PDZ_Class_2 | 382 | 387 | PF00595 | 0.594 |
LIG_SH2_CRK | 220 | 224 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.503 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.529 |
LIG_SUMO_SIM_par_1 | 317 | 324 | PF11976 | 0.510 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.532 |
LIG_UBA3_1 | 154 | 162 | PF00899 | 0.347 |
LIG_WRC_WIRS_1 | 189 | 194 | PF05994 | 0.258 |
LIG_WRC_WIRS_1 | 298 | 303 | PF05994 | 0.606 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.675 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.578 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.783 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.693 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.304 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.221 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.529 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.789 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.811 |
MOD_Cter_Amidation | 257 | 260 | PF01082 | 0.620 |
MOD_Cter_Amidation | 345 | 348 | PF01082 | 0.525 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.278 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.410 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.528 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.558 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.745 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.608 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.736 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.664 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.278 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.327 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.641 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.680 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.656 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.695 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.674 |
MOD_N-GLC_2 | 100 | 102 | PF02516 | 0.269 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.656 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.529 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.289 |
MOD_PK_1 | 111 | 117 | PF00069 | 0.278 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.502 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.276 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.370 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.413 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.596 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.652 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.530 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.428 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.599 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.370 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.300 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.534 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.607 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.698 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.624 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.215 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.612 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.587 |
TRG_NLS_MonoExtC_3 | 69 | 75 | PF00514 | 0.508 |
TRG_NLS_MonoExtN_4 | 47 | 52 | PF00514 | 0.653 |
TRG_NLS_MonoExtN_4 | 69 | 74 | PF00514 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 265 | 270 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7F7 | Leptomonas seymouri | 60% | 100% |
A0A3Q8IE49 | Leishmania donovani | 90% | 99% |
A0A3S7X1K9 | Leishmania donovani | 28% | 100% |
A0A422N066 | Trypanosoma rangeli | 42% | 100% |
A4HH34 | Leishmania braziliensis | 66% | 100% |
A4I3Q4 | Leishmania infantum | 28% | 100% |
A4I485 | Leishmania infantum | 89% | 99% |
C9ZKP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AM46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |