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: E9B228
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_NRD_NRD_1 | 151 | 153 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.600 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.426 |
CLV_PCSK_PC7_1 | 435 | 441 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.433 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.548 |
DOC_CYCLIN_RxL_1 | 91 | 101 | PF00134 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 91 | 98 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.315 |
DOC_PP1_RVXF_1 | 363 | 370 | PF00149 | 0.368 |
DOC_PP1_RVXF_1 | 449 | 455 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.336 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.494 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 399 | 408 | PF00244 | 0.279 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.486 |
LIG_14-3-3_CterR_2 | 460 | 462 | PF00244 | 0.439 |
LIG_APCC_ABBA_1 | 197 | 202 | PF00400 | 0.384 |
LIG_APCC_ABBA_1 | 96 | 101 | PF00400 | 0.306 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.578 |
LIG_BIR_III_2 | 22 | 26 | PF00653 | 0.492 |
LIG_Clathr_ClatBox_1 | 83 | 87 | PF01394 | 0.581 |
LIG_Clathr_ClatBox_1 | 97 | 101 | PF01394 | 0.468 |
LIG_deltaCOP1_diTrp_1 | 129 | 137 | PF00928 | 0.429 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.431 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.471 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.481 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.437 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.423 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.539 |
LIG_LIR_Gen_1 | 136 | 143 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 74 | 84 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.510 |
LIG_NRBOX | 272 | 278 | PF00104 | 0.388 |
LIG_Pex14_1 | 133 | 137 | PF04695 | 0.379 |
LIG_PTAP_UEV_1 | 30 | 35 | PF05743 | 0.657 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.393 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.685 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.510 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.494 |
LIG_SH3_5 | 72 | 76 | PF00018 | 0.472 |
LIG_SUMO_SIM_anti_2 | 302 | 309 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.382 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.547 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.541 |
MOD_CDC14_SPxK_1 | 88 | 91 | PF00782 | 0.476 |
MOD_CDK_SPK_2 | 412 | 417 | PF00069 | 0.444 |
MOD_CDK_SPxK_1 | 85 | 91 | PF00069 | 0.502 |
MOD_CDK_SPxxK_3 | 85 | 92 | PF00069 | 0.496 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.581 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.363 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.298 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.516 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.630 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.502 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.628 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.508 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.436 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.469 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.618 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.444 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.304 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.418 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.488 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.669 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.742 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.524 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.554 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.519 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.602 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.638 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.436 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.503 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.363 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.557 |
MOD_N-GLC_2 | 13 | 15 | PF02516 | 0.454 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.598 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.556 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.400 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.421 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.284 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.441 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.373 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.536 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.337 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.436 |
MOD_Plk_2-3 | 341 | 347 | PF00069 | 0.458 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.405 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.394 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.439 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.339 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.415 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.545 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.490 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.537 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.474 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.502 |
MOD_SUMO_rev_2 | 101 | 109 | PF00179 | 0.545 |
TRG_DiLeu_BaEn_2 | 449 | 455 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_4 | 381 | 387 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 272 | 277 | PF01217 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.580 |
TRG_NES_CRM1_1 | 236 | 250 | PF08389 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXH6 | Leptomonas seymouri | 46% | 100% |
A0A3S7X4Q0 | Leishmania donovani | 83% | 100% |
A4HJL0 | Leishmania braziliensis | 66% | 100% |
A4I710 | Leishmania infantum | 83% | 100% |
Q4Q634 | Leishmania major | 83% | 100% |
V5BA98 | Trypanosoma cruzi | 26% | 100% |