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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HBS4
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_NRD_NRD_1 | 187 | 189 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.722 |
CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.555 |
DEG_APCC_DBOX_1 | 84 | 92 | PF00400 | 0.456 |
DEG_COP1_1 | 97 | 106 | PF00400 | 0.483 |
DEG_SPOP_SBC_1 | 266 | 270 | PF00917 | 0.646 |
DOC_CKS1_1 | 357 | 362 | PF01111 | 0.744 |
DOC_CYCLIN_yCln2_LP_2 | 218 | 224 | PF00134 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 84 | 90 | PF00134 | 0.484 |
DOC_MAPK_gen_1 | 82 | 92 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 82 | 90 | PF00069 | 0.476 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.406 |
DOC_PP2B_LxvP_1 | 253 | 256 | PF13499 | 0.492 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.405 |
DOC_PP2B_LxvP_1 | 90 | 93 | PF13499 | 0.453 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.803 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.626 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 209 | 218 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 307 | 312 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 354 | 358 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 482 | 488 | PF00244 | 0.626 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.716 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.767 |
LIG_deltaCOP1_diTrp_1 | 69 | 75 | PF00928 | 0.489 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.409 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.523 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.797 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.802 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.520 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.422 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.651 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.730 |
LIG_LIR_Gen_1 | 25 | 31 | PF02991 | 0.685 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.700 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.740 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.448 |
LIG_RPA_C_Fungi | 3 | 15 | PF08784 | 0.504 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.778 |
LIG_SH2_NCK_1 | 340 | 344 | PF00017 | 0.713 |
LIG_SH2_NCK_1 | 476 | 480 | PF00017 | 0.778 |
LIG_SH2_PTP2 | 162 | 165 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.769 |
LIG_SH2_STAT3 | 3 | 6 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.690 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.774 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.691 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.777 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.436 |
LIG_SUMO_SIM_par_1 | 267 | 278 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 283 | 289 | PF11976 | 0.552 |
LIG_SxIP_EBH_1 | 123 | 134 | PF03271 | 0.468 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.778 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.548 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.523 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.482 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.345 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.661 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.441 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.632 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.323 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.562 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.811 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.519 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.756 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.748 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.719 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.700 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.495 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.773 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.791 |
MOD_DYRK1A_RPxSP_1 | 333 | 337 | PF00069 | 0.514 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.447 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.646 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.481 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.648 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.669 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.632 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.756 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.599 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.541 |
MOD_GlcNHglycan | 43 | 48 | PF01048 | 0.797 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.645 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.617 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.488 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.729 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.595 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.570 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.596 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.524 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.604 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.712 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.690 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.718 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.718 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.693 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.671 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.746 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.718 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.665 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.548 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.572 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.519 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.492 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.667 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.632 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.729 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.658 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.793 |
MOD_NEK2_2 | 353 | 358 | PF00069 | 0.719 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.787 |
MOD_PK_1 | 271 | 277 | PF00069 | 0.478 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.621 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.694 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.638 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.449 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.519 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.579 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.529 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.613 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.620 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.697 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.709 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.688 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.767 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.688 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.736 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.578 |
MOD_SUMO_rev_2 | 294 | 304 | PF00179 | 0.614 |
MOD_SUMO_rev_2 | 52 | 59 | PF00179 | 0.694 |
MOD_SUMO_rev_2 | 64 | 74 | PF00179 | 0.538 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.738 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.448 |
TRG_NLS_Bipartite_1 | 67 | 86 | PF00514 | 0.552 |
TRG_NLS_MonoExtN_4 | 79 | 86 | PF00514 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P864 | Leptomonas seymouri | 64% | 99% |
A0A3R7KEE9 | Trypanosoma rangeli | 42% | 86% |
A0A3S5H796 | Leishmania donovani | 84% | 98% |
A4HZ78 | Leishmania infantum | 84% | 98% |
D0A1F9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 87% |
E9AV45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% |
Q4QCD6 | Leishmania major | 84% | 100% |
V5BMY3 | Trypanosoma cruzi | 42% | 87% |