GapMind for catabolism of small carbon sources

 

Alignments for a candidate for opuBA in Hippea alviniae EP5-r

Align BusAA, component of Uptake system for glycine-betaine (high affinity) and proline (low affinity) (OpuAA-OpuABC) or BusAA-ABC of Lactococcus lactis). BusAA, the ATPase subunit, has a C-terminal tandem cystathionine β-synthase (CBS) domain which is the cytoplasmic K+ sensor for osmotic stress (osmotic strength)while the BusABC subunit has the membrane and receptor domains fused to each other (Biemans-Oldehinkel et al., 2006; Mahmood et al., 2006; Gul et al. 2012). An N-terminal amphipathic α-helix of OpuA is necessary for high activity but is not critical for biogenesis or the ionic regulation of transport (characterized)
to candidate WP_022670625.1 G415_RS0105555 ABC transporter ATP-binding protein

Query= TCDB::Q9RQ06
         (407 letters)



>NCBI__GCF_000420385.1:WP_022670625.1
          Length = 326

 Score =  142 bits (357), Expect = 2e-38
 Identities = 85/231 (36%), Positives = 136/231 (58%), Gaps = 7/231 (3%)

Query: 44  VYDTNFEINEGEIFVIMGLSGSGKSTLLRLLNRLIEPTSGKIFIDDQDVATLNKEDLLQV 103
           V D +F I +GE   I+G SGSGK+TL R + RL EPT+G I    +D+A L K +L + 
Sbjct: 35  VDDVSFSIRKGETLGIVGESGSGKTTLGRTVLRLTEPTAGSIIFKGKDLAKLPKSELRK- 93

Query: 104 RRKSMSMVFQN--FGLFPHRTILENTEYGLEVQNV-PKEERRKRAEKALDNANLL---DF 157
            RK+  ++FQ+    L P+  I +   + LE+ N+  K ER++R  +  +  NL    +F
Sbjct: 94  ERKNFQIIFQDPMASLNPYMRIGKIVSHPLEIHNIGTKNERKERILELFEKINLSPAEEF 153

Query: 158 KDQYPKQLSGGMQQRVGLARALANDPEILLMDEAFSALDPLIRREMQDELLELQAKFQKT 217
            +++PK LSGG +QRV +ARAL  +PE ++ DE  + LD  +R ++   +++++  F  T
Sbjct: 154 YNRFPKHLSGGQRQRVVIARALITNPEFIVADEPTAMLDVSVRSQILKLMIDVKETFGLT 213

Query: 218 IIFVSHDLNEALRIGDRIAIMKDGKIMQIGTGEEILTNPANDYVKTFVEDV 268
            +F++HDL  A  I DRI +M  GKI++I    ++   P + Y K  +  V
Sbjct: 214 YLFITHDLASAKYICDRIGVMYLGKIVEIAKTFDLFKEPLHPYTKILMSSV 264


Lambda     K      H
   0.316    0.135    0.364 

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: 288
Number of extensions: 13
Number of successful extensions: 2
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: 407
Length of database: 326
Length adjustment: 29
Effective length of query: 378
Effective length of database: 297
Effective search space:   112266
Effective search space used:   112266
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 (21.6 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