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: A0A3S5H796
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 | 0.477 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.349 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.710 |
DEG_APCC_DBOX_1 | 84 | 92 | PF00400 | 0.399 |
DEG_COP1_1 | 97 | 106 | PF00400 | 0.419 |
DEG_SCF_FBW7_1 | 357 | 363 | PF00400 | 0.627 |
DEG_SCF_FBW7_1 | 409 | 414 | PF00400 | 0.628 |
DEG_SPOP_SBC_1 | 266 | 270 | PF00917 | 0.610 |
DOC_CKS1_1 | 357 | 362 | PF01111 | 0.708 |
DOC_CYCLIN_yCln2_LP_2 | 218 | 224 | PF00134 | 0.374 |
DOC_CYCLIN_yCln2_LP_2 | 7 | 13 | PF00134 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 84 | 90 | PF00134 | 0.431 |
DOC_MAPK_gen_1 | 82 | 92 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 82 | 90 | PF00069 | 0.423 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.341 |
DOC_PP2B_LxvP_1 | 253 | 256 | PF13499 | 0.425 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.350 |
DOC_PP2B_LxvP_1 | 90 | 93 | PF13499 | 0.395 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.601 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.592 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.753 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.395 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.571 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 307 | 312 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 358 | 368 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 58 | 66 | PF00244 | 0.418 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.686 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.646 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.721 |
LIG_deltaCOP1_diTrp_1 | 69 | 75 | PF00928 | 0.447 |
LIG_EVH1_2 | 385 | 389 | PF00568 | 0.601 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.352 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.536 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.478 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.682 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.692 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.387 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.577 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.697 |
LIG_LIR_Apic_2 | 25 | 30 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 481 | 492 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 481 | 487 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.399 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.532 |
LIG_SH2_CRK | 484 | 488 | PF00017 | 0.663 |
LIG_SH2_NCK_1 | 340 | 344 | PF00017 | 0.599 |
LIG_SH2_NCK_1 | 484 | 488 | PF00017 | 0.663 |
LIG_SH2_PTP2 | 162 | 165 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.756 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.681 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.665 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.751 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.378 |
LIG_SUMO_SIM_par_1 | 283 | 289 | PF11976 | 0.440 |
LIG_SxIP_EBH_1 | 123 | 134 | PF03271 | 0.412 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.692 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.482 |
LIG_UBA3_1 | 217 | 223 | PF00899 | 0.447 |
LIG_WW_1 | 435 | 438 | PF00397 | 0.671 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.498 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.610 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.578 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.567 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.473 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.681 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.700 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.707 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.673 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.651 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.676 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.624 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.433 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.704 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.736 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.579 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.787 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.709 |
MOD_GlcNHglycan | 43 | 48 | PF01048 | 0.757 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.602 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.668 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.649 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.497 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.526 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.535 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.672 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.642 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.712 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.667 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.680 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.637 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.711 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.619 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.695 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.695 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.485 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.438 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.611 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.604 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.637 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.568 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.677 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.799 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.771 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.629 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.432 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.432 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.394 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.630 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.610 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.471 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.496 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.544 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.567 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.653 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.672 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.651 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.736 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.671 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.687 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.527 |
MOD_SUMO_rev_2 | 294 | 304 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 52 | 59 | PF00179 | 0.628 |
MOD_SUMO_rev_2 | 64 | 74 | PF00179 | 0.433 |
TRG_DiLeu_BaEn_4 | 213 | 219 | PF01217 | 0.348 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.695 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.393 |
TRG_NLS_Bipartite_1 | 67 | 86 | PF00514 | 0.506 |
TRG_NLS_MonoExtN_4 | 79 | 86 | PF00514 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P864 | Leptomonas seymouri | 66% | 100% |
A0A3R7KEE9 | Trypanosoma rangeli | 43% | 87% |
A4HBS4 | Leishmania braziliensis | 84% | 98% |
A4HZ78 | Leishmania infantum | 100% | 100% |
D0A1F9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 88% |
E9AV45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4QCD6 | Leishmania major | 96% | 100% |
V5BMY3 | Trypanosoma cruzi | 45% | 89% |