A large and likely artifical grouping of protease domain carrying proteins related to proteasomal proteases. Only a tiny subgroup (the AFG3-related mitochondrail proteins) seem to have a TM segment.. Localization: Cytoplasmic (by homology) / Mitochondrial (by homology)
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000922 | spindle pole | 2 | 11 |
GO:0005737 | cytoplasm | 2 | 11 |
GO:0005874 | microtubule | 6 | 11 |
GO:0099080 | supramolecular complex | 2 | 11 |
GO:0099081 | supramolecular polymer | 3 | 11 |
GO:0099512 | supramolecular fiber | 4 | 11 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
Related structures:
AlphaFold database: A4H784
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 11 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007010 | cytoskeleton organization | 5 | 11 |
GO:0007017 | microtubule-based process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0051013 | microtubule severing | 4 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008017 | microtubule binding | 5 | 11 |
GO:0008092 | cytoskeletal protein binding | 3 | 11 |
GO:0008568 | microtubule severing ATPase activity | 2 | 11 |
GO:0015631 | tubulin binding | 4 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0140776 | protein-containing complex destabilizing activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.297 |
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.409 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.582 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.409 |
CLV_PCSK_FUR_1 | 130 | 134 | PF00082 | 0.682 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 463 | 465 | PF00082 | 0.297 |
CLV_PCSK_PC7_1 | 459 | 465 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.396 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.716 |
DEG_SCF_FBW7_1 | 140 | 146 | PF00400 | 0.482 |
DEG_SPOP_SBC_1 | 164 | 168 | PF00917 | 0.724 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.482 |
DOC_CYCLIN_RxL_1 | 380 | 387 | PF00134 | 0.297 |
DOC_CYCLIN_RxL_1 | 475 | 486 | PF00134 | 0.464 |
DOC_MAPK_gen_1 | 332 | 340 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 36 | 46 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 380 | 390 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 434 | 443 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 459 | 469 | PF00069 | 0.297 |
DOC_MAPK_HePTP_8 | 35 | 47 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 38 | 47 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 460 | 469 | PF00069 | 0.297 |
DOC_MAPK_RevD_3 | 465 | 481 | PF00069 | 0.474 |
DOC_PP1_RVXF_1 | 473 | 480 | PF00149 | 0.436 |
DOC_PP1_SILK_1 | 328 | 333 | PF00149 | 0.490 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.423 |
DOC_PP4_FxxP_1 | 340 | 343 | PF00568 | 0.297 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.376 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.289 |
LIG_14-3-3_CanoR_1 | 299 | 306 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 359 | 363 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 419 | 429 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 169 | 186 | PF00022 | 0.759 |
LIG_Actin_WH2_2 | 276 | 291 | PF00022 | 0.526 |
LIG_BIR_III_4 | 112 | 116 | PF00653 | 0.723 |
LIG_BRCT_BRCA1_1 | 394 | 398 | PF00533 | 0.297 |
LIG_CaM_IQ_9 | 60 | 75 | PF13499 | 0.497 |
LIG_CtBP_PxDLS_1 | 170 | 174 | PF00389 | 0.637 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.470 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.716 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.508 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.285 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.297 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.340 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.561 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.452 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.214 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.317 |
LIG_Integrin_RGD_1 | 375 | 377 | PF01839 | 0.297 |
LIG_LIR_Apic_2 | 257 | 262 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 297 | 306 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 535 | 545 | PF02991 | 0.189 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 535 | 540 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.405 |
LIG_LYPXL_yS_3 | 323 | 326 | PF13949 | 0.417 |
LIG_Pex14_1 | 577 | 581 | PF04695 | 0.199 |
LIG_Rb_pABgroove_1 | 380 | 388 | PF01858 | 0.340 |
LIG_SH2_CRK | 157 | 161 | PF00017 | 0.506 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.189 |
LIG_SH2_SRC | 392 | 395 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 493 | 497 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.333 |
LIG_SH3_2 | 541 | 546 | PF14604 | 0.425 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.565 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.660 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.370 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.297 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.387 |
LIG_SH3_4 | 270 | 277 | PF00018 | 0.479 |
LIG_SUMO_SIM_anti_2 | 507 | 512 | PF11976 | 0.297 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 42 | 48 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 465 | 471 | PF11976 | 0.465 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.485 |
LIG_TYR_ITIM | 155 | 160 | PF00017 | 0.535 |
LIG_TYR_ITIM | 321 | 326 | PF00017 | 0.404 |
LIG_UBA3_1 | 326 | 335 | PF00899 | 0.405 |
LIG_UBA3_1 | 425 | 434 | PF00899 | 0.317 |
LIG_UBA3_1 | 457 | 463 | PF00899 | 0.297 |
LIG_UBA3_1 | 478 | 485 | PF00899 | 0.284 |
LIG_WRC_WIRS_1 | 92 | 97 | PF05994 | 0.299 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.740 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.742 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.743 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.182 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.304 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.483 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.429 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.731 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.765 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.375 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.212 |
MOD_Cter_Amidation | 240 | 243 | PF01082 | 0.776 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.642 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.566 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.718 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.175 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.370 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.340 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.435 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.549 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.662 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.668 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.428 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.708 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.304 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.282 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.280 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.308 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.388 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.315 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.313 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.288 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.480 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.595 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.177 |
MOD_N-GLC_2 | 159 | 161 | PF02516 | 0.476 |
MOD_N-GLC_2 | 532 | 534 | PF02516 | 0.403 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.517 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.384 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.180 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.297 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.663 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.297 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.409 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.406 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.523 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.730 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.400 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.317 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.370 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.502 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.670 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.481 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.308 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.295 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.285 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.287 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.272 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.394 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.513 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.714 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.289 |
MOD_SUMO_for_1 | 421 | 424 | PF00179 | 0.297 |
MOD_SUMO_rev_2 | 30 | 35 | PF00179 | 0.513 |
TRG_DiLeu_BaEn_1 | 401 | 406 | PF01217 | 0.286 |
TRG_DiLeu_BaEn_1 | 462 | 467 | PF01217 | 0.297 |
TRG_DiLeu_BaEn_4 | 30 | 36 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 478 | 483 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.502 |
TRG_NLS_Bipartite_1 | 419 | 438 | PF00514 | 0.317 |
TRG_NLS_MonoCore_2 | 129 | 134 | PF00514 | 0.617 |
TRG_NLS_MonoExtC_3 | 433 | 439 | PF00514 | 0.317 |
TRG_NLS_MonoExtN_4 | 130 | 135 | PF00514 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 289 | 293 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 521 | 526 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P897 | Leptomonas seymouri | 68% | 100% |
A0A0S4IR32 | Bodo saltans | 53% | 100% |
A0A1X0NPJ1 | Trypanosomatidae | 58% | 100% |
A0A3Q8I9I1 | Leishmania donovani | 82% | 100% |
A0JMA9 | Xenopus tropicalis | 43% | 100% |
A4HVM4 | Leishmania infantum | 82% | 100% |
A9RA82 | Papio anubis | 43% | 100% |
B4JII0 | Drosophila grimshawi | 38% | 75% |
B4M0H8 | Drosophila virilis | 40% | 76% |
B7NZ88 | Oryctolagus cuniculus | 43% | 100% |
D0A6N0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9APC0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q3B8D5 | Xenopus laevis | 38% | 100% |
Q4QG58 | Leishmania major | 80% | 96% |
Q8IYT4 | Homo sapiens | 42% | 100% |
Q9BW62 | Homo sapiens | 43% | 100% |
Q9D3R6 | Mus musculus | 43% | 100% |
V5DBR1 | Trypanosoma cruzi | 56% | 99% |