Align Dihydroxy-acid dehydratase; DAD; EC 4.2.1.9 (uncharacterized)
to candidate WP_085125965.1 B9O00_RS27685 L-arabinonate dehydratase
Query= curated2:B5YKD5 (550 letters) >NCBI__GCF_900177295.1:WP_085125965.1 Length = 586 Score = 337 bits (865), Expect = 6e-97 Identities = 193/539 (35%), Positives = 302/539 (56%), Gaps = 13/539 (2%) Query: 15 HRALLFATGI-PKSEMNKPFIGVATSFTDIIPGHISMKELERFIEKGIHTGGGYPFFFGI 73 HR+ G P+ KP + + +++D P H K +++G+ GG+P Sbjct: 34 HRSRAMQMGYAPEDWAGKPVVAIVNTWSDAQPCHAHFKSRVEDVKRGVFQAGGFPMELPA 93 Query: 74 PGICDGIAMGHKGMKYSLPSRELIADIIECIVEAHQFDGIVLLTNCDKITPGMLMAAARL 133 + + ++ R ++A E ++ +H D VL+ CDK TPG++M A Sbjct: 94 LSLSESFVK-----PTTMLYRNMLAMETEELLRSHPVDAAVLMGGCDKTTPGLVMGALSA 148 Query: 134 DIPAIVLTAGPMLAGYYKGQRRNLTSDTFEAIGKFKKGVLTEKDLEALELCACPGAGSCQ 193 +P I L AGPML G Y+GQ SD ++ + + G L+ + + +E G C Sbjct: 149 GLPMIFLPAGPMLRGNYRGQALGSGSDAWKYWDERRAGNLSAAEWQGVEGGIARSYGHCM 208 Query: 194 GMYTANTMACVTEALGMSLPGTAATPAVMSEKRRLAFETGVKIVELVRKKINARQILTKE 253 M TA+TM + EALG++L G ++ PA + R+A G + VE+ + + ++L Sbjct: 209 TMGTASTMTAIAEALGLTLSGASSIPAADANHIRMASAVGRRAVEMAWEDLTPDRVLDAR 268 Query: 254 AFYNAIAVDMALGGSTNTVLHIKAIANEAGINLPLEVFDEISRKTPHLVNIIPSGEHY-M 312 A NA+ V MA G STN V+H+ A+A AG+ L L+ D SR TP + NI PSG Y M Sbjct: 269 AVRNAVTVAMATGCSTNAVIHLIAMARRAGVPLGLDDLDAASRVTPVIANIRPSGSTYLM 328 Query: 313 EDLYKAGGIPAVLKRLKDKI-YSNPTVSGIDIKEIAQKAEIYDENVIRSIKKAYHKEGGV 371 ED Y AGG+ A++ RL D++ S TVSG + E + AE+YDE+VIRS++ ++EG + Sbjct: 329 EDFYYAGGLRALMARLGDRLDLSAVTVSGRTLGEELEGAEVYDEDVIRSLENPIYQEGSL 388 Query: 372 AILKGNLAPDGAVVKQTAVSSKMLKFEGIARCFDSEENAMKAILDGK--IKEGDVIIIRY 429 A+L+GNLAPDG V+K +A + + + EG A FDS A+ D + DV+++R Sbjct: 389 AVLRGNLAPDGCVIKPSACAPHLRQHEGRALVFDSYPGMKAAVEDESLDVTADDVLVLRN 448 Query: 430 EGPSGGPGMRE--MLSPTSAITGMGLNESVALITDGRFSGGTRGPCIGHVSPEAARGGPI 487 GP GGPGM E ML + G+ + + I+D R SG + G C+ HV+PEA GGP+ Sbjct: 449 AGPRGGPGMPEWGMLPIPKKLVKEGVRDMLR-ISDARMSGTSYGACVLHVAPEACVGGPL 507 Query: 488 AIVKDGDKILIDIPKRKIEILISESEIKKRLKNWKPPKQKIEKGYLLRYARNVSSADKG 546 A+++ GD+I +D+P R I++L+ E+ +R W PP + + +G+ +AR++ AD+G Sbjct: 508 ALLRTGDRIRVDVPARTIDMLVEPEELARRRAAWTPPAETVGRGWNWLFARHIEQADQG 566 Lambda K H 0.318 0.137 0.395 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: 738 Number of extensions: 36 Number of successful extensions: 6 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: 550 Length of database: 586 Length adjustment: 36 Effective length of query: 514 Effective length of database: 550 Effective search space: 282700 Effective search space used: 282700 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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