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: A0A451EJV0
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.628 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.637 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.684 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.805 |
DEG_SPOP_SBC_1 | 176 | 180 | PF00917 | 0.611 |
DOC_CKS1_1 | 432 | 437 | PF01111 | 0.623 |
DOC_MAPK_gen_1 | 130 | 139 | PF00069 | 0.768 |
DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 312 | 322 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 366 | 376 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 267 | 275 | PF00069 | 0.536 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.677 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.791 |
LIG_14-3-3_CanoR_1 | 182 | 191 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 366 | 376 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 421 | 426 | PF00244 | 0.585 |
LIG_Actin_WH2_2 | 351 | 368 | PF00022 | 0.563 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.696 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.622 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.528 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.603 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.641 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.649 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.586 |
LIG_NRBOX | 428 | 434 | PF00104 | 0.592 |
LIG_PTB_Apo_2 | 227 | 234 | PF02174 | 0.543 |
LIG_PTB_Phospho_1 | 227 | 233 | PF10480 | 0.546 |
LIG_SH2_GRB2like | 172 | 175 | PF00017 | 0.623 |
LIG_SH2_SRC | 18 | 21 | PF00017 | 0.699 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 213 | 216 | PF00017 | 0.536 |
LIG_SH2_STAT3 | 232 | 235 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.699 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.738 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.599 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.728 |
LIG_SUMO_SIM_anti_2 | 272 | 277 | PF11976 | 0.525 |
LIG_SUMO_SIM_anti_2 | 334 | 341 | PF11976 | 0.696 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.622 |
LIG_SUMO_SIM_par_1 | 418 | 426 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.570 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.730 |
LIG_UBA3_1 | 429 | 436 | PF00899 | 0.708 |
MOD_CDK_SPK_2 | 423 | 428 | PF00069 | 0.641 |
MOD_CDK_SPK_2 | 431 | 436 | PF00069 | 0.578 |
MOD_CDK_SPK_2 | 88 | 93 | PF00069 | 0.791 |
MOD_CDK_SPxxK_3 | 88 | 95 | PF00069 | 0.795 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.684 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.697 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.704 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.714 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.669 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.519 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.704 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.697 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.641 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.527 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.607 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.696 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.584 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.687 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.377 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.462 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.578 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.658 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.661 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.776 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.760 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.623 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.657 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.609 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.647 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.567 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.732 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.508 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.497 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.567 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.810 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.615 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.625 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.632 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.514 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.780 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.713 |
MOD_NEK2_2 | 125 | 130 | PF00069 | 0.761 |
MOD_NEK2_2 | 30 | 35 | PF00069 | 0.601 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.700 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.533 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.538 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.573 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.509 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.528 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.602 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.571 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.503 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.795 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.411 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.623 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.610 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.692 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.535 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.670 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.793 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.635 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.581 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.706 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.792 |
TRG_DiLeu_BaEn_1 | 115 | 120 | PF01217 | 0.717 |
TRG_DiLeu_BaEn_1 | 266 | 271 | PF01217 | 0.660 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.683 |
TRG_NES_CRM1_1 | 272 | 285 | PF08389 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 340 | 344 | PF00026 | 0.626 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3X9 | Leptomonas seymouri | 64% | 95% |
A4H3S4 | Leishmania braziliensis | 83% | 100% |
A4HRZ9 | Leishmania infantum | 100% | 100% |
E9AJY7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q95Z91 | Leishmania major | 92% | 100% |