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: Q4Q1A4
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 | 0.369 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.259 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.369 |
CLV_Separin_Metazoa | 13 | 17 | PF03568 | 0.325 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.294 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.491 |
DEG_SCF_FBW7_1 | 195 | 202 | PF00400 | 0.546 |
DEG_SCF_FBW7_1 | 337 | 344 | PF00400 | 0.516 |
DEG_SPOP_SBC_1 | 212 | 216 | PF00917 | 0.571 |
DOC_CKS1_1 | 338 | 343 | PF01111 | 0.528 |
DOC_MAPK_MEF2A_6 | 107 | 114 | PF00069 | 0.325 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.613 |
DOC_SPAK_OSR1_1 | 76 | 80 | PF12202 | 0.369 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 117 | 125 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 4 | 14 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 76 | 80 | PF00244 | 0.325 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.604 |
LIG_CtBP_PxDLS_1 | 143 | 147 | PF00389 | 0.579 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.682 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.735 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.328 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.317 |
LIG_LIR_Apic_2 | 186 | 192 | PF02991 | 0.613 |
LIG_LIR_Apic_2 | 307 | 311 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.743 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.369 |
LIG_MYND_1 | 208 | 212 | PF01753 | 0.516 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.304 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.618 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.740 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.633 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.633 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.304 |
LIG_SH3_2 | 173 | 178 | PF14604 | 0.640 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.640 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.500 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.625 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.575 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.595 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.580 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.626 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.640 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.608 |
LIG_SUMO_SIM_par_1 | 396 | 401 | PF11976 | 0.623 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.354 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.693 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.647 |
LIG_WRC_WIRS_1 | 90 | 95 | PF05994 | 0.369 |
LIG_WW_2 | 208 | 211 | PF00397 | 0.522 |
MOD_CDC14_SPxK_1 | 175 | 178 | PF00782 | 0.553 |
MOD_CDK_SPxK_1 | 172 | 178 | PF00069 | 0.607 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.577 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.369 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.192 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.360 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.598 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.340 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.447 |
MOD_GlcNHglycan | 124 | 128 | PF01048 | 0.461 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.637 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.712 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.630 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.614 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.365 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.403 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.295 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.682 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.660 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.614 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.611 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.649 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.546 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.599 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.675 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.667 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.626 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.732 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.634 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.646 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.313 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.403 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.347 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.404 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.670 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.566 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.498 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.527 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.304 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.490 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.369 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.482 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.713 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.570 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.536 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.583 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.607 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.668 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.564 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.531 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.621 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 16 | 20 | PF00026 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P3S6 | Trypanosomatidae | 39% | 93% |
A0A3S7XB38 | Leishmania donovani | 76% | 90% |
A4HPI1 | Leishmania braziliensis | 64% | 99% |
A4IDA3 | Leishmania infantum | 76% | 90% |
E9AT93 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |