GapMind for catabolism of small carbon sources

 

Aligments for a candidate for aatJ in Paraburkholderia bryophila 376MFSha3.1

Align glutamate-aspartate periplasmic-binding protein (characterized)
to candidate H281DRAFT_04270 H281DRAFT_04270 L-glutamate-binding protein /L-aspartate-binding protein

Query= CharProtDB::CH_002441
         (302 letters)



>FitnessBrowser__Burk376:H281DRAFT_04270
          Length = 297

 Score =  391 bits (1004), Expect = e-113
 Identities = 192/302 (63%), Positives = 243/302 (80%), Gaps = 5/302 (1%)

Query: 1   MQLRKPATAILALALSAGLAQADDAAPAAGSTLDKIAKNGVIVVGHRESSVPFSYYDNQQ 60
           M+++K A  +  L L    A A DA      TL KI   GVI +GHRESS+PFSYYD++Q
Sbjct: 1   MKVKKAALLLATLGLFTVGAHAQDAG-----TLKKIKDTGVISLGHRESSIPFSYYDDKQ 55

Query: 61  KVVGYSQDYSNAIVEAVKKKLNKPDLQVKLIPITSQNRIPLLQNGTFDFECGSTTNNVER 120
            V+GYSQ+++  +V+AVK+KLN P+L+VKL P+TSQNRIPL+QNGT D ECGSTTNN ER
Sbjct: 56  NVIGYSQEFALKVVDAVKQKLNMPNLKVKLTPVTSQNRIPLVQNGTVDMECGSTTNNAER 115

Query: 121 QKQAAFSDTIFVVGTRLLTKKGGDIKDFANLKDKAVVVTSGTTSEVLLNKLNEEQKMNMR 180
           Q+Q AFS+TIFV+GTRL+TKK   IKD+A+LK K VV T+GTTSE LL K+N+++ M M 
Sbjct: 116 QQQVAFSNTIFVIGTRLMTKKDSGIKDWADLKGKTVVTTAGTTSERLLRKMNQDKSMGMN 175

Query: 181 IISAKDHGDSFRTLESGRAVAFMMDDALLAGERAKAKKPDNWEIVGKPQSQEAYGCMLRK 240
           IISAKDHG+SF TL +GRA AFMMDDALLAGERAK+  P+++ IVG PQS EAYGCMLRK
Sbjct: 176 IISAKDHGESFLTLSTGRAAAFMMDDALLAGERAKSNTPNDFVIVGAPQSHEAYGCMLRK 235

Query: 241 DDPQFKKLMDDTIAQVQTSGEAEKWFDKWFKNPIPPKNLNMNFELSDEMKALFKEPNDKA 300
           +DP+FKK++DD IA+V+TSGEA++ + KWF+ PIPPK LN+NF  SD++KALFK PNDKA
Sbjct: 236 NDPEFKKVVDDAIAKVETSGEADQIYKKWFETPIPPKGLNLNFPESDDIKALFKSPNDKA 295

Query: 301 LN 302
           ++
Sbjct: 296 ID 297


Lambda     K      H
   0.314    0.130    0.366 

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: 319
Number of extensions: 7
Number of successful extensions: 1
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: 302
Length of database: 297
Length adjustment: 27
Effective length of query: 275
Effective length of database: 270
Effective search space:    74250
Effective search space used:    74250
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 2021. 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 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