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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HPI1
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 8 |
GO:0008047 | enzyme activator activity | 3 | 8 |
GO:0030234 | enzyme regulator activity | 2 | 8 |
GO:0030695 | GTPase regulator activity | 4 | 8 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 8 |
GO:0098772 | molecular function regulator activity | 1 | 8 |
GO:0140677 | molecular function activator activity | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.541 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.430 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.421 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.610 |
DEG_SCF_FBW7_1 | 352 | 357 | PF00400 | 0.565 |
DEG_SPOP_SBC_1 | 185 | 189 | PF00917 | 0.547 |
DEG_SPOP_SBC_1 | 328 | 332 | PF00917 | 0.543 |
DOC_CKS1_1 | 304 | 309 | PF01111 | 0.601 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.670 |
DOC_PP4_MxPP_1 | 305 | 308 | PF00568 | 0.674 |
DOC_SPAK_OSR1_1 | 76 | 80 | PF12202 | 0.501 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.423 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.520 |
LIG_14-3-3_CanoR_1 | 293 | 301 | PF00244 | 0.556 |
LIG_BRCT_BRCA1_1 | 283 | 287 | PF00533 | 0.571 |
LIG_CtBP_PxDLS_1 | 145 | 149 | PF00389 | 0.629 |
LIG_deltaCOP1_diTrp_1 | 384 | 391 | PF00928 | 0.572 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.784 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.405 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.397 |
LIG_LIR_Apic_2 | 204 | 210 | PF02991 | 0.665 |
LIG_LIR_Apic_2 | 384 | 389 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 124 | 131 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 200 | 211 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 124 | 128 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.702 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.433 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.376 |
LIG_Pex14_2 | 203 | 207 | PF04695 | 0.702 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.802 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.759 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.759 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.696 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.558 |
LIG_SH2_STAT3 | 317 | 320 | PF00017 | 0.716 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.376 |
LIG_SH3_2 | 237 | 242 | PF14604 | 0.540 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.479 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.648 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.681 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.703 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.610 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.614 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.654 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.619 |
LIG_SH3_4 | 277 | 284 | PF00018 | 0.559 |
LIG_SUMO_SIM_par_1 | 102 | 108 | PF11976 | 0.229 |
LIG_SUMO_SIM_par_1 | 402 | 407 | PF11976 | 0.685 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.786 |
LIG_TRFH_1 | 154 | 158 | PF08558 | 0.538 |
LIG_WRC_WIRS_1 | 90 | 95 | PF05994 | 0.501 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.765 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.551 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.586 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.614 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.531 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.544 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.436 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.501 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.406 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.636 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.376 |
MOD_GlcNHglycan | 124 | 128 | PF01048 | 0.524 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.765 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.595 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.674 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.725 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.804 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.745 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.734 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.573 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.511 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.396 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.385 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.412 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.692 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.802 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.724 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.455 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.365 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.763 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.786 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.689 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.822 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.744 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.697 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.376 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.494 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.365 |
MOD_NEK2_2 | 354 | 359 | PF00069 | 0.544 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.462 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.692 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.430 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.772 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.639 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.523 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.376 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.527 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.610 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.598 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.365 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.784 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.679 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.758 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.574 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.603 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.584 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.701 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.515 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.596 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.666 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 16 | 20 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P3S6 | Trypanosomatidae | 35% | 94% |
A0A3S7XB38 | Leishmania donovani | 70% | 90% |
A4IDA3 | Leishmania infantum | 70% | 90% |
D0A8E3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AT93 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
Q4Q1A4 | Leishmania major | 64% | 95% |