Align Histidine ammonia-lyase (EC 4.3.1.3) (characterized)
to candidate SMc00669 SMc00669 histidine ammonia-lyase
Query= reanno::pseudo1_N1B4:Pf1N1B4_1582 (507 letters) >FitnessBrowser__Smeli:SMc00669 Length = 499 Score = 419 bits (1076), Expect = e-121 Identities = 234/482 (48%), Positives = 311/482 (64%), Gaps = 4/482 (0%) Query: 6 KIVIADAPLRWQDVVAVARHGAQLELSPQIWTRIENAQAIVQRIVASGERAYGVNTGLGA 65 +++ D PL W+++ ++A GA L+LS RI A+ IV +V G R YG+NTG+GA Sbjct: 3 EMISLDGPLTWREIASIAE-GASLDLSGPARLRIAQARRIVDALVERGIRGYGINTGVGA 61 Query: 66 LCNVSLKGEQLSQLSRNTLLSHACGVGAPLADEQTRAIICAAIRNYSHGKSGIHRRVVEA 125 LC+V + E LSRN +LSHACGVG PL + RA++ A I N +HG SG+ E Sbjct: 62 LCDVIISRENQQALSRNIILSHACGVGDPLGRVEARAVMAAQIANLTHGYSGVRVETAEM 121 Query: 126 LLALLNRGITPQVPSQGSVGYLTHMAHIGITLLGVGNVSYRGQIVTAQQALSEEGLQPVQ 185 LLALLN I P +PS+GSVGYLTH A IG+ L+G G+ + ++ AL+ GL P++ Sbjct: 122 LLALLNADIIPLIPSRGSVGYLTHAAAIGLVLIGHGSAMQGTERLSGADALARLGLAPLR 181 Query: 186 LGAKDGLCLVNGTPCMTGLSCLAIADATRLVQWADVIGAMSFEAQRGQIAAFDAEIIALK 245 L AK+GL LVNGTPC TGL+ LA+A RL WAD AM++E Q AF +AL+ Sbjct: 182 LEAKEGLSLVNGTPCATGLAALALARTERLFAWADAAAAMTYENLGSQANAFAELPLALR 241 Query: 246 PHLGMQQVGINLRALLDGSEVIASSKGIRTQDALSIRSIPQVHGAARDQLEHAKKQIETE 305 G+ VG LR L S ++A + G RTQD LS+R++PQVHGAARD + ++ E Sbjct: 242 QSPGLSAVGEGLRDWLADSPMLAGTAGTRTQDPLSLRAVPQVHGAARDAFGQVAEIVDRE 301 Query: 306 LNSVTDNPMLLGTPDNFRVMSQANPHGQSVALAADLLAIAMAEIGSIAERRLDRLINPHV 365 L SVTDNP + G+P+ V SQA+ G ++ LA D LA+A+AE+ +I+ERR+DRL+NP V Sbjct: 302 LASVTDNPAVAGSPEAPEVHSQAHAVGAALGLAMDSLAVAVAEVAAISERRIDRLVNPLV 361 Query: 366 SGLPAFLVANPGVNSGMMIVQYVAASLCAENRQLAQPAVLDNYVTSGLQEDHLSMGTNAA 425 SGLPAFL + GV+SG MI QY AA+L AENR+LA PA LD +TS LQED L+ T AA Sbjct: 362 SGLPAFLAGDSGVSSGFMIAQYTAAALVAENRRLAAPASLDGGITSALQEDMLTHATPAA 421 Query: 426 LKLHRALENCTQILAIEYLLAAQAFEFLKEQRFGAGTDTA--WRLLRERVPAYDQDRWLA 483 K ++N +ILAIE L AAQA+E L+ Q G TA + +R +PAY DR + Sbjct: 422 WKALSIVDNLERILAIELLAAAQAYE-LQPQAQGKAQRTAALYGHIRSAIPAYRDDRPMN 480 Query: 484 PD 485 D Sbjct: 481 ED 482 Lambda K H 0.319 0.133 0.384 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 644 Number of extensions: 21 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 507 Length of database: 499 Length adjustment: 34 Effective length of query: 473 Effective length of database: 465 Effective search space: 219945 Effective search space used: 219945 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory