GapMind for catabolism of small carbon sources

 

L-histidine catabolism in Pleomorphomonas diazotrophica R5-392

Best path

braC, braD, braE, braF, braG, hutH, hutU, hutI, hutF, hutG'

Rules

Overview: Histidine utilization in GapMind is based on MetaCyc pathways L-histidine degradation I (link) or II (link). These pathways are very similar. Other pathways in MetaCyc (III-VI) are not complete or are not reported in prokaryotes, so they are not included.

48 steps (37 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
braC ABC transporter for glutamate, histidine, arginine, and other amino acids, substrate-binding component BraC CXZ10_RS02245 CXZ10_RS02250
braD ABC transporter for glutamate, histidine, arginine, and other amino acids, permease component 1 (BraD) CXZ10_RS02220 CXZ10_RS20565
braE ABC transporter for glutamate, histidine, arginine, and other amino acids, permease component 2 (BraE) CXZ10_RS02225
braF ABC transporter for glutamate, histidine, arginine, and other amino acids, ATPase component 1 (BraF) CXZ10_RS02230 CXZ10_RS20575
braG ABC transporter for glutamate, histidine, arginine, and other amino acids, ATPase component 2 (BraG) CXZ10_RS02235 CXZ10_RS20580
hutH histidine ammonia-lyase CXZ10_RS19200 CXZ10_RS04085
hutU urocanase CXZ10_RS04045
hutI imidazole-5-propionate hydrolase CXZ10_RS19205
hutF N-formiminoglutamate deiminase CXZ10_RS04060
hutG' N-formylglutamate amidohydrolase CXZ10_RS19195 CXZ10_RS10520
Alternative steps:
aapJ L-histidine ABC transporter, substrate-binding component AapJ CXZ10_RS00830
aapM L-histidine ABC transporter, permease component 2 (AapM) CXZ10_RS00840 CXZ10_RS07640
aapP L-histidine ABC transporter, ATPase component AapP CXZ10_RS00845 CXZ10_RS07645
aapQ L-histidine ABC transporter, permease component 1 (AapQ) CXZ10_RS00835
Ac3H11_2554 ABC transporter for L-Histidine, permease component 2 CXZ10_RS17805 CXZ10_RS12295
Ac3H11_2555 L-histidine ABC transporter, substrate-binding component 2 CXZ10_RS03890 CXZ10_RS17800
Ac3H11_2560 L-histidine ABC transporter, ATPase component CXZ10_RS12725 CXZ10_RS18710
Ac3H11_2561 L-histidine ABC transporter, permease component 1 CXZ10_RS04140 CXZ10_RS07860
Ac3H11_2562 L-histidine ABC transporter, substrate-binding component 1
bgtA L-histidine ABC transporter, ATPase component BgtA CXZ10_RS04080 CXZ10_RS00845
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
BPHYT_RS24000 L-histidine ABC transporter, substrate-binding component CXZ10_RS04065 CXZ10_RS12875
BPHYT_RS24005 L-histidine ABC transporter, permease component 1 CXZ10_RS04070 CXZ10_RS12880
BPHYT_RS24010 L-histidine ABC transporter, permease component 2 CXZ10_RS04075 CXZ10_RS03910
BPHYT_RS24015 L-histidine ABC transporter, ATPase component CXZ10_RS04080 CXZ10_RS07645
Ga0059261_1577 L-histidine transporter CXZ10_RS00535
hisJ L-histidine ABC transporter, substrate-binding component HisJ CXZ10_RS03890 CXZ10_RS12875
hisM L-histidine ABC transporter, permease component 1 (HisM) CXZ10_RS04075 CXZ10_RS12885
hisP L-histidine ABC transporter, ATPase component HisP CXZ10_RS04080 CXZ10_RS00845
hisQ L-histidine ABC transporter, permease component 2 (HisQ) CXZ10_RS04070 CXZ10_RS12880
hutG N-formiminoglutamate formiminohydrolase
hutV L-histidine ABC transporter, ATPase component HutV CXZ10_RS08460 CXZ10_RS12345
hutW L-histidine ABC transporter, permease component HutW CXZ10_RS08455
hutX L-histidine ABC transporter, substrate-binding component HutX
LAT2 L-histidine transporter
LHT L-histidine transporter
natA L-histidine ABC transporter, ATPase component 1 (NatA) CXZ10_RS02230 CXZ10_RS20575
natB L-histidine ABC transporter, substrate-binding component NatB
natC L-histidine ABC transporter, permease component 1 (NatC)
natD L-histidine ABC transporter, permease component 2 (NatD) CXZ10_RS20565
natE L-histidine ABC transporter, ATPase component 2 (NatE) CXZ10_RS02235 CXZ10_RS13695
PA5503 L-histidine ABC transporter, ATPase component CXZ10_RS06880 CXZ10_RS00845
PA5504 L-histidine ABC transporter, permease component CXZ10_RS06885
PA5505 L-histidine ABC transporter, substrate-binding component CXZ10_RS06875
permease L-histidine permease CXZ10_RS00650
PTR2 L-histidine:H+ symporter
S15A3 L-histidine transporter
SLC38A3 L-histidine:Na+ symporter

Confidence: high confidence medium confidence low confidence
transporter – transporters and PTS systems are shaded because predicting their specificity is particularly challenging.

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