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. | yes | 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: A0A3Q8IEE2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.459 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.425 |
DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.428 |
DEG_SPOP_SBC_1 | 272 | 276 | PF00917 | 0.753 |
DOC_MAPK_gen_1 | 134 | 142 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 263 | 273 | PF00069 | 0.651 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.466 |
DOC_MAPK_JIP1_4 | 15 | 21 | PF00069 | 0.575 |
DOC_PP2B_LxvP_1 | 206 | 209 | PF13499 | 0.386 |
DOC_PP4_FxxP_1 | 119 | 122 | PF00568 | 0.420 |
DOC_PP4_FxxP_1 | 179 | 182 | PF00568 | 0.361 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.651 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.656 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 472 | 478 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 503 | 509 | PF00244 | 0.371 |
LIG_APCC_ABBA_1 | 115 | 120 | PF00400 | 0.415 |
LIG_eIF4E_1 | 347 | 353 | PF01652 | 0.586 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.430 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.365 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.532 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.635 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.503 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.523 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.438 |
LIG_Integrin_RGD_1 | 10 | 12 | PF01839 | 0.491 |
LIG_LIR_Apic_2 | 178 | 182 | PF02991 | 0.357 |
LIG_LIR_Apic_2 | 236 | 241 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 67 | 73 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.273 |
LIG_MYND_1 | 26 | 30 | PF01753 | 0.436 |
LIG_PDZ_Class_1 | 549 | 554 | PF00595 | 0.626 |
LIG_Pex14_1 | 151 | 155 | PF04695 | 0.387 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.552 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.321 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 508 | 512 | PF00017 | 0.297 |
LIG_SH2_STAT3 | 118 | 121 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.345 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.527 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.640 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.543 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.696 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.451 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.472 |
LIG_SUMO_SIM_anti_2 | 18 | 24 | PF11976 | 0.588 |
LIG_SUMO_SIM_anti_2 | 32 | 37 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 15 | 20 | PF11976 | 0.610 |
LIG_SUMO_SIM_par_1 | 171 | 178 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 221 | 227 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 485 | 491 | PF11976 | 0.451 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.393 |
LIG_WRC_WIRS_1 | 339 | 344 | PF05994 | 0.617 |
MOD_CDC14_SPxK_1 | 548 | 551 | PF00782 | 0.684 |
MOD_CDK_SPK_2 | 252 | 257 | PF00069 | 0.702 |
MOD_CDK_SPxK_1 | 545 | 551 | PF00069 | 0.679 |
MOD_CDK_SPxxK_3 | 178 | 185 | PF00069 | 0.342 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.650 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.598 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.754 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.717 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.648 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.491 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.424 |
MOD_DYRK1A_RPxSP_1 | 309 | 313 | PF00069 | 0.645 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.449 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.617 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.691 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.622 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.640 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.581 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.508 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.392 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.466 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.647 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.716 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.745 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.755 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.582 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.347 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.584 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.604 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.432 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.749 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.496 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.534 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.636 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.593 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.380 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.500 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.489 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.421 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.435 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.625 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.553 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.508 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.503 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.377 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.819 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.373 |
MOD_PKB_1 | 336 | 344 | PF00069 | 0.608 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.462 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.425 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.483 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.629 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.402 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.476 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.358 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.685 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.700 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.679 |
MOD_SUMO_rev_2 | 12 | 17 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 488 | 495 | PF00179 | 0.430 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 444 | 446 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 452 | 455 | PF00400 | 0.473 |
TRG_NES_CRM1_1 | 346 | 362 | PF08389 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HS69 | Leptomonas seymouri | 62% | 94% |
A0A0S4KE41 | Bodo saltans | 44% | 100% |
A4HIZ0 | Leishmania braziliensis | 84% | 100% |
A4I4P4 | Leishmania infantum | 100% | 100% |
E9AE47 | Leishmania major | 95% | 100% |
E9ALN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |