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: E9ATL0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.785 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.712 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.446 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.474 |
DEG_MDM2_SWIB_1 | 211 | 219 | PF02201 | 0.419 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.672 |
DOC_CYCLIN_RxL_1 | 172 | 183 | PF00134 | 0.440 |
DOC_CYCLIN_RxL_1 | 254 | 265 | PF00134 | 0.473 |
DOC_MAPK_gen_1 | 124 | 130 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 338 | 348 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 366 | 374 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 340 | 348 | PF00069 | 0.455 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.574 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 187 | 194 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 303 | 307 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.635 |
LIG_Actin_WH2_2 | 241 | 259 | PF00022 | 0.523 |
LIG_Actin_WH2_2 | 396 | 414 | PF00022 | 0.503 |
LIG_AP_GAE_1 | 116 | 122 | PF02883 | 0.605 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.487 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.557 |
LIG_eIF4E_1 | 164 | 170 | PF01652 | 0.436 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.690 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.686 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.455 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.630 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.663 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.481 |
LIG_Integrin_RGD_1 | 85 | 87 | PF01839 | 0.807 |
LIG_Integrin_RGD_1 | 91 | 93 | PF01839 | 0.694 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.531 |
LIG_NRBOX | 343 | 349 | PF00104 | 0.456 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.414 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.596 |
LIG_SH2_GRB2like | 351 | 354 | PF00017 | 0.443 |
LIG_SH2_SRC | 351 | 354 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.567 |
LIG_SH2_STAT3 | 103 | 106 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 168 | 171 | PF00017 | 0.535 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.338 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.763 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.689 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.703 |
LIG_SUMO_SIM_anti_2 | 146 | 153 | PF11976 | 0.547 |
LIG_SUMO_SIM_anti_2 | 230 | 235 | PF11976 | 0.542 |
LIG_SUMO_SIM_anti_2 | 343 | 348 | PF11976 | 0.428 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.465 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.491 |
LIG_TRFH_1 | 103 | 107 | PF08558 | 0.475 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.620 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.598 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.525 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.445 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.759 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.540 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.583 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.716 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.785 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.608 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.505 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.510 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.561 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.502 |
MOD_GlcNHglycan | 383 | 387 | PF01048 | 0.544 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.526 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.712 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.721 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.708 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.762 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.642 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.693 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.442 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.509 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.664 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.747 |
MOD_LATS_1 | 185 | 191 | PF00433 | 0.470 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.525 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.696 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.526 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.518 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.462 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.568 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.576 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.782 |
MOD_NEK2_2 | 302 | 307 | PF00069 | 0.575 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.599 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.588 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.681 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.503 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.580 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.551 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.629 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.757 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.638 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.765 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.580 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.477 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.673 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.729 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.592 |
TRG_DiLeu_BaEn_1 | 343 | 348 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_4 | 195 | 201 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 251 | 256 | PF01217 | 0.600 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 175 | 180 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 197 | 201 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 332 | 337 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J8 | Leptomonas seymouri | 66% | 100% |
A0A0S4JG62 | Bodo saltans | 50% | 100% |
A0A1X0P1T1 | Trypanosomatidae | 52% | 100% |
A0A3Q8ILB9 | Leishmania donovani | 90% | 100% |
A0A422P583 | Trypanosoma rangeli | 55% | 100% |
A4HPU5 | Leishmania braziliensis | 78% | 100% |
A4IE48 | Leishmania infantum | 90% | 100% |
Q4Q0Y8 | Leishmania major | 88% | 100% |
V5BQ98 | Trypanosoma cruzi | 57% | 100% |