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: E9APC0
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 | 112 | 116 | PF00656 | 0.688 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.504 |
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.254 |
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.383 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.542 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.383 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 433 | 435 | PF00082 | 0.254 |
CLV_PCSK_PC7_1 | 127 | 133 | PF00082 | 0.533 |
CLV_PCSK_PC7_1 | 429 | 435 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.362 |
DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.503 |
DEG_Kelch_Keap1_1 | 121 | 126 | PF01344 | 0.459 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.635 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.671 |
DOC_CYCLIN_RxL_1 | 350 | 357 | PF00134 | 0.254 |
DOC_CYCLIN_RxL_1 | 445 | 456 | PF00134 | 0.432 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 161 | 170 | PF00134 | 0.691 |
DOC_MAPK_gen_1 | 302 | 310 | PF00069 | 0.315 |
DOC_MAPK_gen_1 | 350 | 360 | PF00069 | 0.273 |
DOC_MAPK_gen_1 | 36 | 46 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 404 | 413 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 429 | 439 | PF00069 | 0.254 |
DOC_MAPK_HePTP_8 | 35 | 47 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 38 | 47 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 430 | 439 | PF00069 | 0.254 |
DOC_MAPK_RevD_3 | 435 | 451 | PF00069 | 0.453 |
DOC_PP1_RVXF_1 | 443 | 450 | PF00149 | 0.402 |
DOC_PP1_SILK_1 | 298 | 303 | PF00149 | 0.455 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.254 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.294 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.350 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 107 | 117 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 133 | 139 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 329 | 333 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 389 | 399 | PF00244 | 0.254 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 533 | 537 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.494 |
LIG_Actin_WH2_2 | 147 | 164 | PF00022 | 0.674 |
LIG_Actin_WH2_2 | 246 | 261 | PF00022 | 0.506 |
LIG_AP2alpha_2 | 229 | 231 | PF02296 | 0.460 |
LIG_BIR_III_4 | 113 | 117 | PF00653 | 0.668 |
LIG_BRCT_BRCA1_1 | 364 | 368 | PF00533 | 0.254 |
LIG_CaM_IQ_9 | 21 | 36 | PF13499 | 0.331 |
LIG_CaM_IQ_9 | 60 | 75 | PF13499 | 0.580 |
LIG_CtBP_PxDLS_1 | 148 | 152 | PF00389 | 0.595 |
LIG_EVH1_1 | 242 | 246 | PF00568 | 0.462 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.384 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.479 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.254 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.254 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.301 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.513 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.447 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.177 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.387 |
LIG_Integrin_isoDGR_2 | 502 | 504 | PF01839 | 0.383 |
LIG_Integrin_RGD_1 | 345 | 347 | PF01839 | 0.254 |
LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.415 |
LIG_LYPXL_yS_3 | 293 | 296 | PF13949 | 0.404 |
LIG_MYND_1 | 159 | 163 | PF01753 | 0.674 |
LIG_Rb_pABgroove_1 | 350 | 358 | PF01858 | 0.298 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.273 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.297 |
LIG_SH3_1 | 240 | 246 | PF00018 | 0.450 |
LIG_SH3_2 | 511 | 516 | PF14604 | 0.661 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.627 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.543 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.469 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.353 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.270 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.621 |
LIG_SUMO_SIM_anti_2 | 17 | 24 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 477 | 482 | PF11976 | 0.254 |
LIG_SUMO_SIM_anti_2 | 81 | 88 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 42 | 48 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 435 | 441 | PF11976 | 0.383 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.465 |
LIG_TYR_ITIM | 291 | 296 | PF00017 | 0.367 |
LIG_UBA3_1 | 296 | 305 | PF00899 | 0.365 |
LIG_UBA3_1 | 395 | 404 | PF00899 | 0.273 |
LIG_UBA3_1 | 427 | 433 | PF00899 | 0.254 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.576 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.709 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.265 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.264 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.522 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.484 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.416 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.762 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.679 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.345 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.177 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.392 |
MOD_Cter_Amidation | 211 | 214 | PF01082 | 0.692 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.621 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.621 |
MOD_GlcNHglycan | 187 | 191 | PF01048 | 0.663 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.758 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.591 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.472 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.292 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.296 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.409 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.598 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.681 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.665 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.254 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.254 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.271 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.262 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.283 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.453 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.358 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.454 |
MOD_LATS_1 | 507 | 513 | PF00433 | 0.647 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.770 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.323 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.348 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.254 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.646 |
MOD_NEK2_2 | 328 | 333 | PF00069 | 0.254 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.495 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.387 |
MOD_PIKK_1 | 492 | 498 | PF00454 | 0.294 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.713 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.295 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.333 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.489 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.494 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.581 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.454 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.264 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.254 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.254 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.254 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.254 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.405 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.713 |
MOD_SUMO_for_1 | 391 | 394 | PF00179 | 0.254 |
MOD_SUMO_rev_2 | 30 | 35 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.254 |
TRG_DiLeu_BaEn_1 | 432 | 437 | PF01217 | 0.254 |
TRG_DiLeu_BaEn_4 | 30 | 36 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 448 | 453 | PF01217 | 0.417 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 131 | 133 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.476 |
TRG_NLS_Bipartite_1 | 389 | 408 | PF00514 | 0.273 |
TRG_NLS_MonoExtC_3 | 403 | 409 | PF00514 | 0.273 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.254 |
TRG_Pf-PMV_PEXEL_1 | 491 | 496 | PF00026 | 0.333 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P897 | Leptomonas seymouri | 68% | 97% |
A0A0S4IR32 | Bodo saltans | 54% | 100% |
A0A1X0NPJ1 | Trypanosomatidae | 59% | 97% |
A0A3Q8I9I1 | Leishmania donovani | 91% | 99% |
A0JMA9 | Xenopus tropicalis | 44% | 100% |
A4H784 | Leishmania braziliensis | 80% | 100% |
A4HVM4 | Leishmania infantum | 91% | 99% |
C9ZK16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 68% |
D0A6N0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 98% |
Q3B8D5 | Xenopus laevis | 38% | 100% |
Q4QG58 | Leishmania major | 91% | 100% |
Q5XIK7 | Rattus norvegicus | 43% | 100% |
Q6AZT2 | Xenopus laevis | 37% | 93% |
Q8IYT4 | Homo sapiens | 41% | 100% |
Q9D3R6 | Mus musculus | 41% | 100% |
V5DBR1 | Trypanosoma cruzi | 57% | 94% |