Metal Binding, TPR-repeat
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. | yes | yes: 10 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0101031 | protein folding chaperone complex | 3 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I340
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.465 |
CLV_PCSK_FUR_1 | 298 | 302 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.297 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.424 |
DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.570 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.289 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.268 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.561 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.741 |
DEG_SPOP_SBC_1 | 349 | 353 | PF00917 | 0.749 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.513 |
DOC_CKS1_1 | 471 | 476 | PF01111 | 0.513 |
DOC_MAPK_gen_1 | 227 | 233 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 297 | 307 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 444 | 452 | PF00069 | 0.456 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.630 |
DOC_USP7_UBL2_3 | 173 | 177 | PF12436 | 0.367 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.500 |
LIG_APCC_ABBA_1 | 448 | 453 | PF00400 | 0.409 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.445 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.449 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.447 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.399 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.664 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.503 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.509 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.636 |
LIG_LIR_Gen_1 | 374 | 382 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 393 | 401 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.411 |
LIG_PCNA_PIPBox_1 | 388 | 397 | PF02747 | 0.534 |
LIG_Pex14_2 | 378 | 382 | PF04695 | 0.440 |
LIG_SH2_GRB2like | 131 | 134 | PF00017 | 0.406 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.390 |
LIG_SH2_PTP2 | 395 | 398 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.430 |
LIG_SH3_1 | 468 | 474 | PF00018 | 0.572 |
LIG_SH3_2 | 471 | 476 | PF14604 | 0.591 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.698 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.527 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.621 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 303 | 312 | PF11976 | 0.674 |
LIG_SUMO_SIM_anti_2 | 462 | 469 | PF11976 | 0.435 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.512 |
LIG_TRAF2_1 | 232 | 235 | PF00917 | 0.401 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.636 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.614 |
LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.750 |
LIG_UBA3_1 | 416 | 425 | PF00899 | 0.429 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.515 |
LIG_WW_2 | 336 | 339 | PF00397 | 0.493 |
MOD_CDK_SPK_2 | 368 | 373 | PF00069 | 0.469 |
MOD_CDK_SPxK_1 | 470 | 476 | PF00069 | 0.503 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.449 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.636 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.645 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.642 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.461 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.485 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.609 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.441 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.518 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.734 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.283 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.479 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.522 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.521 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.332 |
MOD_GlcNHglycan | 195 | 199 | PF01048 | 0.409 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.701 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.636 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.692 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.691 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.509 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.571 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.609 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.590 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.634 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.657 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.632 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.496 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.493 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.386 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.240 |
MOD_N-GLC_1 | 427 | 432 | PF02516 | 0.240 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.613 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.478 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.521 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.477 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.298 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.442 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.559 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.511 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.524 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.535 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.609 |
MOD_Plk_2-3 | 235 | 241 | PF00069 | 0.686 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.712 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.630 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.573 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.633 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.433 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.440 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.503 |
MOD_SUMO_rev_2 | 13 | 23 | PF00179 | 0.474 |
MOD_SUMO_rev_2 | 311 | 321 | PF00179 | 0.701 |
MOD_SUMO_rev_2 | 477 | 485 | PF00179 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 394 | 399 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.409 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.515 |
TRG_ER_diLys_1 | 484 | 488 | PF00400 | 0.529 |
TRG_NLS_Bipartite_1 | 212 | 232 | PF00514 | 0.616 |
TRG_NLS_MonoCore_2 | 226 | 231 | PF00514 | 0.602 |
TRG_NLS_MonoExtC_3 | 296 | 301 | PF00514 | 0.572 |
TRG_NLS_MonoExtN_4 | 227 | 232 | PF00514 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.251 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF88 | Leptomonas seymouri | 62% | 99% |
A0A0S4J9Z5 | Bodo saltans | 40% | 100% |
A0A1X0NH58 | Trypanosomatidae | 39% | 100% |
A0A3Q8IHU4 | Leishmania donovani | 99% | 100% |
A0A3R7KY85 | Trypanosoma rangeli | 38% | 100% |
A4HG19 | Leishmania braziliensis | 83% | 100% |
C9ZJL2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ACV9 | Leishmania major | 94% | 100% |
E9AZE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q28IV3 | Xenopus tropicalis | 25% | 74% |
Q68FQ7 | Rattus norvegicus | 26% | 74% |
Q6NU95 | Xenopus laevis | 26% | 74% |
Q9D706 | Mus musculus | 25% | 74% |
V5AR46 | Trypanosoma cruzi | 39% | 100% |