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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005777 | peroxisome | 6 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ALN8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 10 | 14 | PF00656 | 0.437 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.455 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.410 |
DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.412 |
DOC_MAPK_gen_1 | 134 | 142 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 262 | 273 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.448 |
DOC_MAPK_JIP1_4 | 15 | 21 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 266 | 275 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 466 | 473 | PF00069 | 0.383 |
DOC_PP2B_LxvP_1 | 206 | 209 | PF13499 | 0.373 |
DOC_PP2B_LxvP_1 | 273 | 276 | PF13499 | 0.495 |
DOC_PP4_FxxP_1 | 119 | 122 | PF00568 | 0.406 |
DOC_PP4_FxxP_1 | 179 | 182 | PF00568 | 0.339 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.635 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.625 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 472 | 478 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.487 |
LIG_APCC_ABBA_1 | 115 | 120 | PF00400 | 0.391 |
LIG_eIF4E_1 | 347 | 353 | PF01652 | 0.533 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.416 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.345 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.522 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.624 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.450 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.615 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.425 |
LIG_LIR_Apic_2 | 178 | 182 | PF02991 | 0.338 |
LIG_LIR_Apic_2 | 236 | 241 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 67 | 73 | PF02991 | 0.355 |
LIG_LIR_LC3C_4 | 467 | 471 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.327 |
LIG_MYND_1 | 26 | 30 | PF01753 | 0.431 |
LIG_PDZ_Class_1 | 549 | 554 | PF00595 | 0.610 |
LIG_Pex14_1 | 151 | 155 | PF04695 | 0.376 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.307 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.367 |
LIG_SH2_STAT3 | 118 | 121 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.333 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.518 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.623 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.664 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.422 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.459 |
LIG_SUMO_SIM_anti_2 | 18 | 24 | PF11976 | 0.543 |
LIG_SUMO_SIM_anti_2 | 32 | 37 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 467 | 472 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 15 | 20 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 171 | 178 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 221 | 227 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 271 | 279 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 485 | 491 | PF11976 | 0.433 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.378 |
LIG_WRC_WIRS_1 | 339 | 344 | PF05994 | 0.586 |
MOD_CDC14_SPxK_1 | 548 | 551 | PF00782 | 0.650 |
MOD_CDK_SPK_2 | 252 | 257 | PF00069 | 0.665 |
MOD_CDK_SPxK_1 | 264 | 270 | PF00069 | 0.494 |
MOD_CDK_SPxK_1 | 545 | 551 | PF00069 | 0.644 |
MOD_CDK_SPxxK_3 | 178 | 185 | PF00069 | 0.323 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.630 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.734 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.728 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.626 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.480 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.273 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.498 |
MOD_DYRK1A_RPxSP_1 | 309 | 313 | PF00069 | 0.624 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.448 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.610 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.675 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.609 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.632 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.594 |
MOD_GlcNHglycan | 527 | 531 | PF01048 | 0.404 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.604 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.478 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.350 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.417 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.623 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.692 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.706 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.743 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.488 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.602 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.332 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.549 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.580 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.401 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.525 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.730 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.461 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.457 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.521 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.594 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.316 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.459 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.454 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.406 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.385 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.616 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.570 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.498 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.457 |
MOD_PKA_1 | 262 | 268 | PF00069 | 0.576 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.366 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.503 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.364 |
MOD_PKB_1 | 336 | 344 | PF00069 | 0.584 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.544 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.411 |
MOD_Plk_1 | 526 | 532 | PF00069 | 0.287 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.459 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.619 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.389 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.439 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.236 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.339 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.668 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.529 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.671 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.644 |
MOD_SUMO_for_1 | 26 | 29 | PF00179 | 0.374 |
MOD_SUMO_rev_2 | 10 | 17 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 488 | 495 | PF00179 | 0.412 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 444 | 446 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 452 | 455 | PF00400 | 0.459 |
TRG_NES_CRM1_1 | 346 | 362 | PF08389 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.488 |
TRG_PTS1 | 551 | 554 | PF00515 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HS69 | Leptomonas seymouri | 63% | 94% |
A0A0S4KE41 | Bodo saltans | 43% | 100% |
A0A3Q8IEE2 | Leishmania donovani | 94% | 100% |
A4HIZ0 | Leishmania braziliensis | 82% | 100% |
A4I4P4 | Leishmania infantum | 94% | 100% |
E9AE47 | Leishmania major | 93% | 100% |