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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HN43
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.619 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.474 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 394 | 396 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.617 |
CLV_Separin_Metazoa | 338 | 342 | PF03568 | 0.565 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.726 |
DOC_MAPK_gen_1 | 166 | 174 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 184 | 191 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 346 | 352 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 166 | 174 | PF00069 | 0.471 |
DOC_PP1_RVXF_1 | 127 | 134 | PF00149 | 0.670 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.625 |
LIG_14-3-3_CanoR_1 | 16 | 24 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 184 | 191 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 211 | 219 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 412 | 422 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.414 |
LIG_Actin_WH2_2 | 66 | 83 | PF00022 | 0.490 |
LIG_APCC_ABBA_1 | 318 | 323 | PF00400 | 0.405 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.609 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.596 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.485 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.529 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.596 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.539 |
LIG_LIR_Gen_1 | 130 | 141 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 186 | 194 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 374 | 382 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.357 |
LIG_SH2_CRK | 188 | 192 | PF00017 | 0.532 |
LIG_SH2_NCK_1 | 54 | 58 | PF00017 | 0.659 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.491 |
LIG_SUMO_SIM_par_1 | 170 | 175 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 348 | 353 | PF11976 | 0.505 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.603 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.582 |
LIG_UBA3_1 | 349 | 354 | PF00899 | 0.515 |
LIG_WRC_WIRS_1 | 327 | 332 | PF05994 | 0.627 |
LIG_WW_1 | 427 | 430 | PF00397 | 0.462 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.594 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.604 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.550 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.491 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.458 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.372 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.622 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.554 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.525 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.608 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.532 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.463 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.619 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.401 |
MOD_Cter_Amidation | 126 | 129 | PF01082 | 0.682 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.601 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.570 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.573 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.627 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.612 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.609 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.510 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.509 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.569 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.567 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.567 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.368 |
MOD_N-GLC_2 | 193 | 195 | PF02516 | 0.611 |
MOD_N-GLC_2 | 322 | 324 | PF02516 | 0.382 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.514 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.537 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.520 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.538 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.564 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.543 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.524 |
MOD_NEK2_2 | 326 | 331 | PF00069 | 0.622 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.482 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.372 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.634 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.557 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.602 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.580 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.412 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.508 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.614 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.618 |
MOD_Plk_2-3 | 2 | 8 | PF00069 | 0.624 |
MOD_Plk_2-3 | 34 | 40 | PF00069 | 0.606 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.569 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.613 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.592 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.638 |
MOD_SUMO_for_1 | 165 | 168 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 150 | 160 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 247 | 256 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 356 | 366 | PF00179 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 328 | 333 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.495 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 283 | 287 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ51 | Leptomonas seymouri | 69% | 100% |
A0A0S4JDF0 | Bodo saltans | 37% | 99% |
A0A1X0P5H1 | Trypanosomatidae | 43% | 100% |
A0A3Q8IFE4 | Leishmania donovani | 81% | 100% |
A0A3R7N172 | Trypanosoma rangeli | 45% | 100% |
A4IBR1 | Leishmania infantum | 81% | 100% |
C9ZYW3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AFJ6 | Leishmania major | 81% | 100% |
E9B6Q0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
V5BXZ9 | Trypanosoma cruzi | 41% | 100% |