GapMind for catabolism of small carbon sources

 

Alignments for a candidate for adh in Geotalea uraniireducens Rf4

Align Alcohol dehydrogenase; EC 1.1.1.1; EC 1.1.1.4; EC 1.2.1.3 (characterized)
to candidate WP_011941123.1 GURA_RS22135 NAD(P)-dependent alcohol dehydrogenase

Query= SwissProt::Q0KDL6
         (366 letters)



>NCBI__GCF_000016745.1:WP_011941123.1
          Length = 354

 Score =  303 bits (775), Expect = 6e-87
 Identities = 161/365 (44%), Positives = 220/365 (60%), Gaps = 16/365 (4%)

Query: 1   MTAMMKAAVFVEPGRIELADKPIPDIGPNDALVRITTTTICGTDVHILKGEYPVAKGLTV 60
           M   MKA V      + + ++PIP+ GPNDA+++ T   +C +DVH + G     +   +
Sbjct: 1   MKKSMKAFVMKGINDVGIVERPIPEPGPNDAIIKTTLAMVCTSDVHTVAGGLGEIRDRVL 60

Query: 61  GHEPVGIIEKLGSAVTGYREGQRVIAGAICPNFNSYAAQDGVASQDGSYLMASGQCGCHG 120
           GHE VGI+ KLGSAV G +EG RV   AI P +     Q G  SQ    L          
Sbjct: 61  GHEAVGIVYKLGSAVKGLKEGDRVAVNAITPCYKCENCQRGFPSQCTVML---------- 110

Query: 121 YKATAGWRFGNMIDGTQAEYVLVPDAQANLTPIPDGLTDEQVLMCPDIMSTGFKGAENAN 180
                G++F    DG  AEY  V DA+AN+ PIP G++DE      D+MSTGFKGAENAN
Sbjct: 111 ----GGYKFTTQKDGNLAEYFHVNDAEANVAPIPAGVSDEAACYATDMMSTGFKGAENAN 166

Query: 181 IRIGDTVAVFAQGPIGLCATAGARLCGATTIIAIDGNDHRLEIARKMGADVVLNFRNCDV 240
           I +G +  +F  GP+GL A AG RL GA  +IA+D    RL++A++ GADV +NF+  DV
Sbjct: 167 IPLGGSGVIFGLGPVGLMAVAGTRLLGAGLVIAVDCVPSRLKLAKEYGADVTINFKEQDV 226

Query: 241 VDEVMKLTGGRGVDASIEALGTQATFEQSLRVLKPGGTLSSLGVYSSD--LTIPLSAFAA 298
           V EV++LTGG+G DA++EALG QATFE   +V +PGGT+S++G +     + IP   +  
Sbjct: 227 VAEVLRLTGGQGADAAMEALGAQATFENCFKVTRPGGTISNIGYWGHGDYVNIPRLEWGV 286

Query: 299 GLGDHKINTALCPGGKERMRRLINVIESGRVDLGALVTHQYRLDDIVAAYDLFANQRDGV 358
           G+G+  I T LCPGG ERM RL+ +IE+GRVD   L TH +   D+  A ++   + DG+
Sbjct: 287 GMGEKTIKTLLCPGGSERMGRLMRIIENGRVDPTRLTTHHFSFADVEKALEMMTTKTDGI 346

Query: 359 LKIAI 363
           LK  I
Sbjct: 347 LKPVI 351


Lambda     K      H
   0.320    0.138    0.408 

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: 388
Number of extensions: 15
Number of successful extensions: 3
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: 366
Length of database: 354
Length adjustment: 29
Effective length of query: 337
Effective length of database: 325
Effective search space:   109525
Effective search space used:   109525
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: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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