GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Acidovorax sp. GW101-3H11

Align L-lactate oxidase (EC 1.1.3.2) (characterized)
to candidate Ac3H11_1767 L-lactate dehydrogenase (EC 1.1.2.3)

Query= BRENDA::Q8Z0C8
         (365 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1767
          Length = 419

 Score =  219 bits (559), Expect = 8e-62
 Identities = 139/376 (36%), Positives = 205/376 (54%), Gaps = 32/376 (8%)

Query: 8   INLFEYEQLAKTHLSQMAFDYYISGAGDEITLQENRAVFERIKLRPRMLVDVSQINLTTS 67
           ++L ++E  A+  L +  F Y    A D  +L++NR VF       R+L DVSQ +    
Sbjct: 41  LSLHDFEDAARRRLPRPIFGYIAGAAEDNASLRDNREVFGEYAFTTRVLRDVSQRSQAVE 100

Query: 68  VLGQPLQLPLLIAPMAFQCLAHTEGELATAMAAASAGTGMVLSTLSTKSLEEVAEVGSKF 127
           + G+    P  IAPM    L+   G+L  A AA  AG   V+S  S   +EEVA    + 
Sbjct: 101 LFGERYSSPFGIAPMGINALSTYRGDLVLACAAQRAGIVSVMSGTSLIPMEEVA----RE 156

Query: 128 SPSLQWFQLYIHKDRGLTRALVERAYAAGYKALCLTVDAPVLGQRERDRRNEFVLP--PG 185
           SP   WFQ Y+  D+    AL++R   AG++ L +TVD P+   RE + R  F  P  PG
Sbjct: 157 SPGT-WFQAYLPGDQARIDALIDRVERAGFRTLVVTVDIPISANRENNIRTGFSTPLRPG 215

Query: 186 LHLA-------------NLTTISGLNIPHAPGESGLFTYFAQQLNPA----------LTW 222
           L LA              + T+    +PH   E+   T  A  ++ +          L+W
Sbjct: 216 LRLAWDGLVRPRWVAGTFVRTLLRHGMPHF--ENSFATRGAPIVSSSVLRDFSARDHLSW 273

Query: 223 DDLEWLQSLSPLPLVLKGILRGDDAARAVEYGAKAIVVSNHGGRQLDGAIASLDALPEIV 282
           + LE ++     PLV+KG+LR +DA +A   GA  +V+SNHGGRQLDGA++++  L  +V
Sbjct: 274 NHLEAIRRRWKGPLVVKGVLRVEDALQARNLGADGVVLSNHGGRQLDGAVSAMRVLEAVV 333

Query: 283 AAVNGKAEVLLDGGIRRGTDIIKALAIGAQAVLIGRPVLWGLAVGGQAGVSHVISLLQKE 342
           AAV     VL+DGG RRG+D++KA+A+GA+ VL+GRP  +  AV G+AGV H I LL+ E
Sbjct: 334 AAVGPAFPVLIDGGFRRGSDVLKAIALGARMVLVGRPFNYAAAVAGEAGVQHAIGLLRDE 393

Query: 343 LNVAMALIGCSQLQDI 358
           ++  +A++G     D+
Sbjct: 394 VDRNLAMLGARACTDL 409


Lambda     K      H
   0.320    0.136    0.391 

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: 355
Number of extensions: 17
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 365
Length of database: 419
Length adjustment: 31
Effective length of query: 334
Effective length of database: 388
Effective search space:   129592
Effective search space used:   129592
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: 50 (23.9 bits)

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

Links

Downloads

Related tools

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