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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3S7X4J0
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0003676 | nucleic acid binding | 3 | 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 | 293 | 297 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.552 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.553 |
DEG_APCC_DBOX_1 | 320 | 328 | PF00400 | 0.475 |
DOC_MAPK_gen_1 | 174 | 182 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 218 | 227 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 232 | 241 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 218 | 227 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 373 | 381 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.328 |
DOC_PP1_RVXF_1 | 199 | 205 | PF00149 | 0.511 |
DOC_PP1_RVXF_1 | 72 | 79 | PF00149 | 0.415 |
DOC_PP2B_LxvP_1 | 383 | 386 | PF13499 | 0.413 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.524 |
DOC_USP7_UBL2_3 | 330 | 334 | PF12436 | 0.485 |
DOC_USP7_UBL2_3 | 417 | 421 | PF12436 | 0.308 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 453 | 457 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 82 | 89 | PF00244 | 0.448 |
LIG_AP2alpha_2 | 69 | 71 | PF02296 | 0.394 |
LIG_BRCT_BRCA1_1 | 178 | 182 | PF00533 | 0.441 |
LIG_deltaCOP1_diTrp_1 | 439 | 446 | PF00928 | 0.372 |
LIG_eIF4E_1 | 286 | 292 | PF01652 | 0.444 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.441 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.453 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.509 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.405 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.675 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.496 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.383 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.359 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.417 |
LIG_GBD_Chelix_1 | 52 | 60 | PF00786 | 0.438 |
LIG_Integrin_isoDGR_2 | 281 | 283 | PF01839 | 0.493 |
LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 179 | 187 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 354 | 365 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 77 | 84 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.460 |
LIG_NRBOX | 122 | 128 | PF00104 | 0.486 |
LIG_Pex14_1 | 36 | 40 | PF04695 | 0.351 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.511 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.522 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.529 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 80 | 84 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.312 |
LIG_SH3_1 | 454 | 460 | PF00018 | 0.586 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.419 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.686 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.598 |
LIG_TYR_ITIM | 462 | 467 | PF00017 | 0.526 |
LIG_UBA3_1 | 176 | 181 | PF00899 | 0.327 |
LIG_WRC_WIRS_1 | 204 | 209 | PF05994 | 0.547 |
MOD_CDC14_SPxK_1 | 45 | 48 | PF00782 | 0.471 |
MOD_CDK_SPxK_1 | 42 | 48 | PF00069 | 0.531 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.468 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.498 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.571 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.553 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.505 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.326 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.636 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.696 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.598 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.445 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.383 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.350 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.736 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.512 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.507 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.454 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.447 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.289 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.521 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.414 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.520 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.651 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.503 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.477 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.206 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.616 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.487 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.464 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.500 |
MOD_N-GLC_2 | 261 | 263 | PF02516 | 0.525 |
MOD_N-GLC_2 | 445 | 447 | PF02516 | 0.350 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.530 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.312 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.293 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.543 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.405 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.437 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.289 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.400 |
MOD_NEK2_2 | 159 | 164 | PF00069 | 0.353 |
MOD_NEK2_2 | 425 | 430 | PF00069 | 0.308 |
MOD_OFUCOSY | 407 | 412 | PF10250 | 0.474 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.568 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.636 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.753 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.417 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.416 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.534 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.431 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.343 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.301 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.610 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.439 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.319 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.498 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.483 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.569 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.476 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.302 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.638 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.735 |
MOD_SUMO_for_1 | 329 | 332 | PF00179 | 0.471 |
MOD_SUMO_rev_2 | 331 | 336 | PF00179 | 0.536 |
TRG_DiLeu_BaEn_1 | 119 | 124 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJJ2 | Leptomonas seymouri | 79% | 100% |
A0A0S4JQ55 | Bodo saltans | 30% | 71% |
A0A1X0NPU0 | Trypanosomatidae | 35% | 99% |
A0A3R7M2S8 | Trypanosoma rangeli | 35% | 98% |
A4HJE7 | Leishmania braziliensis | 93% | 100% |
A4I6U2 | Leishmania infantum | 100% | 100% |
C9ZMB3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 93% |
E9B1W5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
Q4Q697 | Leishmania major | 99% | 100% |
V5B432 | Trypanosoma cruzi | 36% | 98% |