GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaE in Cupriavidus basilensis 4G11

Align 1,2-phenylacetyl-CoA epoxidase, subunit E; 1,2-phenylacetyl-CoA epoxidase, reductase subunit; 1,2-phenylacetyl-CoA monooxygenase, subunit E; EC 1.-.-.- (characterized)
to candidate RR42_RS10060 RR42_RS10060 ferredoxin:oxidoreductase FAD/NAD(P)-binding protein

Query= SwissProt::P76081
         (356 letters)



>FitnessBrowser__Cup4G11:RR42_RS10060
          Length = 339

 Score =  181 bits (458), Expect = 3e-50
 Identities = 126/353 (35%), Positives = 175/353 (49%), Gaps = 22/353 (6%)

Query: 4   FHSLTVAKVESETRDAVTITFAVPQPLQEAYRFRPGQHLTLKASFDGEELRRCYSICRSY 63
           FH+LTVA++  ET DA +    VP  LQ+++ +R GQHLT + + DG+ L R YS+  S 
Sbjct: 3   FHNLTVAQITWETEDARSYALLVPDALQQSFVYRAGQHLTFRVNVDGKTLLRSYSLSSSP 62

Query: 64  LPGEISVA-VKAIEGGRFSRYAREHIRQGMTLEVMVPQGHFGYQPQAERQGRYLAI-AAG 121
             G + V  VK I GGR S +   H+  G  LEV  P G F      E  G  L   AAG
Sbjct: 63  EAGGLPVVTVKRIPGGRASGWFHAHVDAGTRLEVSAPTGRF----VCEDMGAPLFFCAAG 118

Query: 122 SGITPMLAIIATTLQTEPESQFTLIYGNRTSQSMMFRQALADLKDKYPQRLQLLCIFSQE 181
           SGITP+L++I + L +   S  TL Y NR + S +F   +A L   +  RL +       
Sbjct: 119 SGITPVLSMIRSALAST-SSAMTLYYANRDAASTIFAAQIAKLSRDHSDRLAV------- 170

Query: 182 TLDSDLLHGRIDGEKLQSLGASLINFRLYDEAFICGPAAMMDDAETALKALGMPDKTIHL 241
                L H   DG   +   A+L++   + + ++CGP   M     A +  GM    +HL
Sbjct: 171 ----HLHHDDTDGFPERGKIAALLSAVPHCQLYLCGPGPFMQTVLEAAEVAGMGPGCVHL 226

Query: 242 ERFNTPGTR--VKRSVNVQSDGQKVTVRQDGRDREIVLNADDESILDAALRQGADLPYAC 299
           ERF+       V  +  + +     TV   G    +V  A  +S+L AAL  G D PYAC
Sbjct: 227 ERFDAAAQEPEVASAAPMPAQACDATVTLGGA-LHVVRVASGQSLLQAALACGVDAPYAC 285

Query: 300 KGGVCATCKCKVLRGKVAMETNYSLEPDELAAGYVLSCQALPLTS-DVVVDFD 351
           + G C +C  K + G V    N     DELAAG++L+CQA P     V + FD
Sbjct: 286 EEGYCGSCAAKCVDGAVVHARNDVFSADELAAGWILTCQARPRQERPVAITFD 338


Lambda     K      H
   0.320    0.135    0.390 

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: 304
Number of extensions: 15
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: 356
Length of database: 339
Length adjustment: 29
Effective length of query: 327
Effective length of database: 310
Effective search space:   101370
Effective search space used:   101370
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: 49 (23.5 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:

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