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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9ACD3
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0030544 | Hsp70 protein binding | 4 | 11 |
GO:0031072 | heat shock protein binding | 3 | 11 |
GO:0051879 | Hsp90 protein binding | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.764 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.764 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.558 |
CLV_Separin_Metazoa | 412 | 416 | PF03568 | 0.567 |
DEG_SPOP_SBC_1 | 173 | 177 | PF00917 | 0.523 |
DEG_SPOP_SBC_1 | 308 | 312 | PF00917 | 0.786 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.686 |
DOC_PP1_RVXF_1 | 107 | 114 | PF00149 | 0.720 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.746 |
DOC_PP4_FxxP_1 | 477 | 480 | PF00568 | 0.712 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.711 |
DOC_USP7_MATH_2 | 488 | 494 | PF00917 | 0.542 |
DOC_USP7_UBL2_3 | 395 | 399 | PF12436 | 0.732 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 102 | 108 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 220 | 225 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 261 | 266 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 287 | 291 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 394 | 398 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 423 | 432 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 445 | 454 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 468 | 477 | PF00244 | 0.733 |
LIG_Actin_WH2_2 | 71 | 88 | PF00022 | 0.635 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.602 |
LIG_BRCT_BRCA1_1 | 473 | 477 | PF00533 | 0.544 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.409 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.538 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.655 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.670 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.693 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.591 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.510 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.757 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.728 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.655 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.621 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.778 |
LIG_LIR_Apic_2 | 474 | 480 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 237 | 242 | PF02991 | 0.343 |
LIG_MYND_1 | 463 | 467 | PF01753 | 0.721 |
LIG_Pex14_1 | 228 | 232 | PF04695 | 0.306 |
LIG_PTB_Apo_2 | 147 | 154 | PF02174 | 0.453 |
LIG_RPA_C_Fungi | 268 | 280 | PF08784 | 0.533 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.721 |
LIG_SH2_GRB2like | 190 | 193 | PF00017 | 0.441 |
LIG_SH2_NCK_1 | 52 | 56 | PF00017 | 0.721 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 211 | 215 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.348 |
LIG_SH2_STAT3 | 232 | 235 | PF00017 | 0.306 |
LIG_SH2_STAT3 | 368 | 371 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.525 |
LIG_SH3_2 | 463 | 468 | PF14604 | 0.726 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.568 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.705 |
LIG_SUMO_SIM_anti_2 | 182 | 187 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 182 | 187 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 219 | 227 | PF11976 | 0.498 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.596 |
LIG_WW_3 | 465 | 469 | PF00397 | 0.735 |
MOD_CDK_SPxxK_3 | 382 | 389 | PF00069 | 0.527 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.680 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.471 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.343 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.461 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.638 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.655 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.657 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.699 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.750 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.752 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.749 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.761 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.570 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.733 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.689 |
MOD_Cter_Amidation | 337 | 340 | PF01082 | 0.638 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.619 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.674 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.568 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.385 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.256 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.693 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.698 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.544 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.679 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.686 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.681 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.729 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.743 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.649 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.713 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.570 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.507 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.454 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.545 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.635 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.736 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.725 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.710 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.622 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.726 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.729 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.643 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.726 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.719 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.718 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.728 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.463 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.340 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.528 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.748 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.729 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.529 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.443 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.563 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.463 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.592 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.680 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.645 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.699 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.671 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.538 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.687 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.772 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.749 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.745 |
MOD_PK_1 | 415 | 421 | PF00069 | 0.677 |
MOD_PKA_1 | 339 | 345 | PF00069 | 0.630 |
MOD_PKA_1 | 468 | 474 | PF00069 | 0.753 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.443 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.477 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.650 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.672 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.686 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.726 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.754 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.785 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.673 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.458 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.502 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.532 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.540 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.742 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.453 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.462 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.523 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.731 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.774 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.718 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.660 |
MOD_SUMO_for_1 | 352 | 355 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 142 | 148 | PF00179 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 499 | 504 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 467 | 470 | PF00400 | 0.741 |
TRG_ER_diArg_1 | 507 | 510 | PF00400 | 0.494 |
TRG_NLS_MonoCore_2 | 507 | 512 | PF00514 | 0.556 |
TRG_NLS_MonoExtN_4 | 508 | 513 | PF00514 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 502 | 506 | PF00026 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0B2 | Leptomonas seymouri | 50% | 92% |
A0A1X0NJW2 | Trypanosomatidae | 34% | 100% |
A0A3S5H509 | Leishmania donovani | 93% | 98% |
A0A422NAY7 | Trypanosoma rangeli | 30% | 100% |
A4H3F0 | Leishmania braziliensis | 72% | 98% |
A4HRQ4 | Leishmania infantum | 93% | 98% |
C9ZJ44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AJM1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 98% |
V5B5N7 | Trypanosoma cruzi | 34% | 100% |