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: 3 |
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: 1, no: 6 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HJL0
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0000774 | adenyl-nucleotide exchange factor activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0060590 | ATPase regulator activity | 2 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.473 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.428 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.546 |
DEG_SCF_FBW7_1 | 186 | 192 | PF00400 | 0.498 |
DOC_CKS1_1 | 111 | 116 | PF01111 | 0.423 |
DOC_CKS1_1 | 186 | 191 | PF01111 | 0.504 |
DOC_CYCLIN_RxL_1 | 312 | 319 | PF00134 | 0.362 |
DOC_CYCLIN_RxL_1 | 91 | 101 | PF00134 | 0.419 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.431 |
DOC_MAPK_gen_1 | 451 | 457 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 91 | 98 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 92 | 99 | PF00149 | 0.464 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.329 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.493 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 151 | 160 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 257 | 267 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 269 | 274 | PF00244 | 0.239 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.502 |
LIG_AP2alpha_1 | 454 | 458 | PF02296 | 0.294 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.598 |
LIG_Clathr_ClatBox_1 | 97 | 101 | PF01394 | 0.468 |
LIG_deltaCOP1_diTrp_1 | 129 | 137 | PF00928 | 0.436 |
LIG_DLG_GKlike_1 | 269 | 276 | PF00625 | 0.268 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.424 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.541 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.488 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.698 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.581 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.435 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.447 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.525 |
LIG_IRF3_LxIS_1 | 158 | 163 | PF10401 | 0.370 |
LIG_LIR_Gen_1 | 136 | 143 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 74 | 84 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.524 |
LIG_NRBOX | 272 | 278 | PF00104 | 0.396 |
LIG_Pex14_1 | 133 | 137 | PF04695 | 0.387 |
LIG_Pex14_2 | 454 | 458 | PF04695 | 0.294 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.391 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.470 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.376 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.670 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.490 |
LIG_SH3_5 | 72 | 76 | PF00018 | 0.491 |
LIG_SUMO_SIM_anti_2 | 201 | 207 | PF11976 | 0.248 |
LIG_SUMO_SIM_anti_2 | 301 | 310 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 243 | 250 | PF11976 | 0.355 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.507 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.560 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.605 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.528 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.543 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.492 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.610 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.312 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.490 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.551 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.443 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.540 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.577 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.565 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.672 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.501 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.487 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.415 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.544 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.300 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.487 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.658 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.669 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.379 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.750 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.583 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.641 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.701 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.537 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.559 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.527 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.331 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.340 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.611 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.378 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.619 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.573 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.427 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.317 |
MOD_N-GLC_2 | 13 | 15 | PF02516 | 0.503 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.574 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.542 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.408 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.455 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.420 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.350 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.464 |
MOD_OFUCOSY | 388 | 394 | PF10250 | 0.291 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.430 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.269 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.545 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.540 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.270 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.317 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.363 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.460 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.418 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.412 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.246 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.336 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.449 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.509 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.491 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.554 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.591 |
TRG_DiLeu_BaEn_2 | 449 | 455 | PF01217 | 0.416 |
TRG_DiLeu_BaEn_4 | 381 | 387 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.372 |
TRG_DiLeu_BaLyEn_6 | 272 | 277 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXH6 | Leptomonas seymouri | 47% | 100% |
A0A3S7X4Q0 | Leishmania donovani | 65% | 100% |
A4I710 | Leishmania infantum | 65% | 100% |
E9B228 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
Q4Q634 | Leishmania major | 66% | 100% |
V5BA98 | Trypanosoma cruzi | 27% | 100% |