Aligments for a candidate for dddA in Marinobacter adhaerens HP15

GapMind for catabolism of small carbon sources

Aligments for a candidate for dddA in Marinobacter adhaerens HP15

Align 3-hydroxypropionate dehydrogenase (EC 1.1.1.59) (characterized)
to candidate GFF4208 HP15_4148 glucose-methanol-choline oxidoreductase

Query= metacyc::MONOMER-15202
         (579 letters)



>lcl|FitnessBrowser__Marino:GFF4208 HP15_4148
           glucose-methanol-choline oxidoreductase
          Length = 542

 Score =  344 bits (883), Expect = 5e-99
 Identities = 216/549 (39%), Positives = 293/549 (53%), Gaps = 20/549 (3%)

Query: 34  HAFDYIVVGAGTAGCLLANRLSADPANRVLLIEAGGRDNYHWIHIPVGYLYCINNPRTDW 93
           ++FDYIVVGAG+AGC+LA+RLSAD    V ++EAG       I  P  +   +     +W
Sbjct: 4   NSFDYIVVGAGSAGCVLADRLSADGRYSVCVLEAGPGKGSFTIRTPGAFAAHMFIKTYNW 63

Query: 94  RFRTEPDPGLNG-RSLIYPRGKTLGGCSSINGMLYLRGQARDYDGWAELTGDDAWRWDNC 152
            F   PD  L G + L  PRGK LGG S INGMLY+RGQ  DYD W E  G++ W +   
Sbjct: 64  AFNARPDQQLRGGQPLFTPRGKGLGGSSLINGMLYVRGQKEDYDEW-EALGNEGWGYAEM 122

Query: 153 LPDFMRHEDHYRLDEGGDADPDHYKFHGHGGEWRI-EKQRLKWQVLADFATAAVEAGVPR 211
           LP F++ E H  L            +HG GG   I   +  ++ +   F  AA + G P 
Sbjct: 123 LPYFLKSEHHETLAGT--------PYHGKGGNLYIGAPETAEYPMSGAFVDAARQTGFPY 174

Query: 212 TRDFNRGDNEGVDAFEVNQRSGWRWNASKAFLRGVEQRGNLTVWHSTQVLKLDFASGEGS 271
           + DFN  + EGV  F +N ++G R+  + A+L+    R NLTV    +V KL     EG+
Sbjct: 175 SSDFNGAEQEGVGYFHLNIKNGRRFGVADAYLKPAMSRQNLTVLTEARVKKLVL---EGN 231

Query: 272 EPRCCGVTVERAGKKVVTTARCEVVLSAGAIGSPQLLQLSGIGPTALLAEHAIPVVADLP 331
             R   V +      +V  A  E++LS GAI SPQLLQLSGIG    L    I    +LP
Sbjct: 232 --RAVAVELRHKDSDLVLNANREIILSGGAINSPQLLQLSGIGDHDALESLGIRCRHELP 289

Query: 332 GVGENLQDHLQIRSIYKVKGAKTLNTMANSLIGKAKIGLEYILKRSGPMSMAPSQLCIFT 391
           GVG+NLQ+H+    +   +           L+      + Y L + G ++ + ++   F 
Sbjct: 290 GVGKNLQEHVDACVLVSSRKNNGFTASLGGLLKMVPDTIRYFLSKRGKLAKSITEAGGFI 349

Query: 392 RSSKEYEHPNLEYHVQPLSLEAFGQPLH--DFPAITASVCNLNPTSRGTVRIKSGNPRQA 449
           +SS     P+++ H+ PL  +  G+ L     P  +  VC L P S GTV I S +P  A
Sbjct: 350 KSSDSVNRPDVQLHMLPLLFDDSGRDLKLMSNPGYSVHVCVLRPKSSGTVTITSADPFAA 409

Query: 450 PAISPNYLSTEEDRQVAADSLRVTRHIASQPAFAKYDPEEFKPGVQYQSDEDLARLAGDI 509
           P I  N+ +  +D +V  D +R  R I +  AF  Y  EE  PG   QSDE +     + 
Sbjct: 410 PEIDYNFFADPDDCKVMVDGIRQARRILAAKAFDDYRGEELHPGADRQSDEQIIEKVKEK 469

Query: 510 GTTIFHPVGTAKMGRDDDPMAVVDSHLRVRGVTGLRVVDASIMPTITSGNTNSPTLMIAE 569
              ++HPVGT KMG   D MAVVD  LRV G+ GLRVVDASIMP + SGNTN+PT+ IAE
Sbjct: 470 VGLVYHPVGTCKMG--TDRMAVVDPQLRVHGLGGLRVVDASIMPRLISGNTNAPTIAIAE 527

Query: 570 KAAGWILKS 578
           KAA  IL++
Sbjct: 528 KAADMILET 536


Lambda     K      H
   0.318    0.135    0.418 

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: 871
Number of extensions: 52
Number of successful extensions: 7
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: 579
Length of database: 542
Length adjustment: 36
Effective length of query: 543
Effective length of database: 506
Effective search space:   274758
Effective search space used:   274758
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 Sep 17 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources