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: A4IDA3
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 | 0.411 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.550 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.323 |
CLV_Separin_Metazoa | 13 | 17 | PF03568 | 0.436 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.598 |
DEG_SPOP_SBC_1 | 193 | 197 | PF00917 | 0.637 |
DOC_CKS1_1 | 304 | 309 | PF01111 | 0.580 |
DOC_CYCLIN_yCln2_LP_2 | 215 | 221 | PF00134 | 0.599 |
DOC_MAPK_MEF2A_6 | 107 | 114 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 109 | 115 | PF00149 | 0.338 |
DOC_PP2B_LxvP_1 | 215 | 218 | PF13499 | 0.607 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.620 |
DOC_SPAK_OSR1_1 | 76 | 80 | PF12202 | 0.513 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.539 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 4 | 14 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 76 | 80 | PF00244 | 0.436 |
LIG_BRCT_BRCA1_1 | 388 | 392 | PF00533 | 0.680 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.776 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.472 |
LIG_IBAR_NPY_1 | 339 | 341 | PF08397 | 0.625 |
LIG_LIR_Apic_2 | 327 | 333 | PF02991 | 0.613 |
LIG_LIR_Apic_2 | 352 | 356 | PF02991 | 0.709 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.785 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.513 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.411 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.679 |
LIG_PTAP_UEV_1 | 332 | 337 | PF05743 | 0.575 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.798 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.746 |
LIG_SH2_NCK_1 | 381 | 385 | PF00017 | 0.746 |
LIG_SH2_STAT3 | 297 | 300 | PF00017 | 0.726 |
LIG_SH2_STAT3 | 341 | 344 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.411 |
LIG_SH3_1 | 381 | 387 | PF00018 | 0.571 |
LIG_SH3_2 | 173 | 178 | PF14604 | 0.744 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.745 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.500 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.632 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.663 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.633 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.685 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.600 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.605 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.595 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.725 |
LIG_SH3_3 | 456 | 462 | PF00018 | 0.685 |
LIG_SUMO_SIM_par_1 | 144 | 149 | PF11976 | 0.626 |
LIG_SUMO_SIM_par_1 | 445 | 450 | PF11976 | 0.733 |
LIG_SxIP_EBH_1 | 433 | 445 | PF03271 | 0.577 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.767 |
LIG_TRAF2_1 | 424 | 427 | PF00917 | 0.762 |
LIG_TRFH_1 | 413 | 417 | PF08558 | 0.551 |
LIG_WRC_WIRS_1 | 90 | 95 | PF05994 | 0.513 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.690 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.725 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.596 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.590 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.596 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.655 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.613 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.459 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.513 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.690 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.411 |
MOD_GlcNHglycan | 124 | 128 | PF01048 | 0.590 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.715 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.717 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.788 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.597 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.611 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.734 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.474 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.692 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.410 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.323 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.740 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.677 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.743 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.550 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.713 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.680 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.512 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.377 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.795 |
MOD_N-GLC_1 | 435 | 440 | PF02516 | 0.583 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.793 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.578 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.812 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.734 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.746 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.387 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.603 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.377 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.474 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.759 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.513 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.747 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.636 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.588 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.552 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.411 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.612 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.436 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.622 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.622 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.377 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.579 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.565 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.776 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.662 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.796 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.583 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.690 |
TRG_DiLeu_BaEn_2 | 114 | 120 | PF01217 | 0.299 |
TRG_DiLeu_BaEn_4 | 115 | 121 | PF01217 | 0.299 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.677 |
TRG_Pf-PMV_PEXEL_1 | 118 | 123 | PF00026 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 16 | 20 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P3S6 | Trypanosomatidae | 39% | 100% |
A0A3S7XB38 | Leishmania donovani | 99% | 100% |
A4HPI1 | Leishmania braziliensis | 70% | 100% |
E9AT93 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q1A4 | Leishmania major | 76% | 89% |