GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaK in Novosphingobium barchaimii LL02

Align medium-chain acyl-CoA ligase (EC 6.2.1.2); phenylacetate-CoA ligase (EC 6.2.1.30) (characterized)
to candidate WP_059153145.1 V474_RS19880 AMP-binding protein

Query= BRENDA::O74725
         (578 letters)



>NCBI__GCF_001046635.1:WP_059153145.1
          Length = 520

 Score =  147 bits (370), Expect = 1e-39
 Identities = 122/365 (33%), Positives = 182/365 (49%), Gaps = 34/365 (9%)

Query: 209 VCYSSGTSGLPKGVMISHRNVIANTL-QIKAFEQNYRDGGGTKPASTEVA-LGLLPQSHI 266
           + YS GT+G PKG+M +HR    +TL Q+ ++E              EV  L   P SH 
Sbjct: 171 IAYSGGTTGKPKGIMTTHRAAATSTLIQLTSWEW-----------PKEVRHLICAPLSHS 219

Query: 267 YALVVIGHAGAYRGDQTIVLPKFELKSYLNAIQQYKISALFLVPPIIIHMLGTQDVCSKY 326
            A V+   A   +G   +VLP F+    + AI  ++I+++ +VP +++ M+       ++
Sbjct: 220 GAAVL--SAVLVKGGSMVVLPGFDPVGTMQAIADHRITSVLMVPTMVLAMIDHPRF-GEF 276

Query: 327 DLSSVTSLFTGAAPLGMETAADFL-KLYPNILIRQGYGLTETCTVVSSTH--PHDI---- 379
           DLSS+  +F GA+        + + KL P  +  Q YG  E    V+      HD+    
Sbjct: 277 DLSSLEVIFYGASAFPTARLKEAIGKLGP--IFFQFYGQAEAPMSVTLLRRDEHDVDDMT 334

Query: 380 WLGSSGALLPGVEARIVTPENKEITTYDSPGELVVRSPSVVLGYLNNEKATAETFVDGWM 439
            L S G   P V   ++     E+   + PGE+ VR P ++ GYLN  + TA  F  GW+
Sbjct: 335 RLSSCGRPSPLVRVALLDDACNEVPEGE-PGEICVRGPLLMAGYLNKPEETAAAFEGGWL 393

Query: 440 RTGDEAVIRRSPKGIEHVFIVDRIKELIKVKGLQVAPAELEAHILAHPDVSDCAVIAIPD 499
            TGD AV  RSP G   + IVDR K++I   G  V   E+E  ++ HP V   AVI +PD
Sbjct: 394 HTGDVAV--RSPDGF--LRIVDRKKDMIVTGGFNVYAREVEDVLVEHPGVRQAAVIGVPD 449

Query: 500 DRAGEVPKAIVVKSASAGSDESVSQALVKYVEDHKARHKWLKGGIRFVDAIPKSPSGKIL 559
           ++ GE  KA+VV       D    QAL+  V + K   +  K  + FVD +P SP GK  
Sbjct: 450 EKWGEAVKAVVVLEPGVEVD---PQALIARVREKKGAVQAPK-TVEFVDELPLSPLGKPD 505

Query: 560 RRLIR 564
           ++ +R
Sbjct: 506 KKALR 510


Lambda     K      H
   0.316    0.134    0.392 

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: 651
Number of extensions: 21
Number of successful extensions: 5
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: 578
Length of database: 520
Length adjustment: 36
Effective length of query: 542
Effective length of database: 484
Effective search space:   262328
Effective search space used:   262328
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: 53 (25.0 bits)

This GapMind analysis is from Sep 24 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:

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